F-Term-List

C07B31/00-61/00@Z;63/00-63/04;C07C1/00-409/44

AA00
TYPE OF INVENTION

AA01

AA02

AA03

AA04

AA05

. Substances

. Methods of preparation (separation purification or stabilisation)

. Uses

. Apparatus

. Others (transport storage or decomposition)

C07C1/00-409/44

AB00
USE

AB01

AB02

AB03

AB04

AB05

AB06

AB10

. Agricultural chemicals (fertilisers)

. . Pesticides or rodenticides

. . Disinfectants or antifungal agents

. . Herbicides

. . Pest repellents or attractants

. . Plant growth regulators

. Food or feed materials (feed additives)

AB12

AB14

AB20

. Cosmetics or shampoos

. Perfumes and applications thereof

. Pharmaceuticals (diagnostic products or antiallergic agents)

AB21

AB22

AB23

AB24

AB25

AB26

AB27

AB28

AB29

. . Pharmaceuticals acting on central nervous systems (sedatives antipyretics or analgesics)

. . Antiinflammatory agents

. . Pharmaceuticals acting on circulatory organs (Vasodilators antihypertensives or anti-arteriosclerotic agents)

. . Pharmaceuticals acting on hematopoietic organs blood or body liquids (anticoagulants or haemostatic agents)

. . Pharmaceuticals acting on respiratory organs (antiasthmatic or antitussive agents)

. . Pharmaceuticals acting on digestive organs (antiulcer agents)

. . Pharmaceuticals acting on metabolic systems (vitamin-like agents hypolipidemic agents or hypoglycemic agents)

. . Antineoplastic agents (carcinostatic agents)

. . Antibacterial agents or antiviral agents

AB40

. Catalysts or reaction aids (reaction initiators)

AB42

AB44

AB46

AB48

AB49

AB50

. Explosives gunpowders or propellants

. Fuels

. Monomers for polymerisation

. Additives for macromolecular compounds

. . Curing agents

. . Plasticisers

AB51

AB60

. . Deterioration preventing agents

. Lubricants (working fluids)

AB61

AB64

AB66

AB68

AB70

. . Additives

. Liquid crystals and applications thereof

. Antistatic additives

. Surfactants (foaming agents defoaming agents emulsifiers solubilising agents dispersants wetting agents coagulants water-repelling or oil-repelling agents)

. Cleaning agents

AB72

AB74

AB76

AB78

AB80

. Fibre or paper materials (sizing agents)

. Building materials (cement admixtures)

. Photographic materials or printing materials (photosensitive agents for photographic purposes sensitising agents or inks)

. Electric materials or communication materials (insulating oils)

. using chemical characteristics (fire prevention agents disaster prevention agents flame retardants or solvents)

AB81

AB82

AB83

AB84

AB90

. . Reaction reagents (oxidising agents reducing agents or optical resolution agents)

. . Chelating agents

. . Stabilisers (antioxidants)

. . Synthesis intermediates

. using physical characteristics (viscosity regulators)

AB91

AB92

AB93

AB99

. . Electric or magnetic characteristics

. . Optical characteristics (infra-red absorbents ultra-violet absorbents or X-ray absorbents luminescent materials or tenebrescence compounds)

. . Thermal characteristics (heat storage agents heat transfer materials coolants or heat-resistant agents)

. Others (paints dyes or adhesives)

C07B31/00-61/00@Z;63/00-63/04;C07C1/00-409/44

AC00
REACTION

AC10

. Changes in forms of carbon-to-carbon bonds (C-C) neither involving formation nor cutting of C-C bonds

AC11

AC12

AC13

AC14

AC20

. . Reduction (benzene to cyclohexane (C6H10) carbon-to-carbon triple bonds to vinylene bonds (-CH=CH-))

. . Dehydrogenation (cyclohexane to benzene ethylene bonds to vinylene bonds (-CH2CH2- to -CH=CH-))

. . Decomposition (carbon-to-halogen carbon-to-oxygen carbon-to-nitrogen carbon-to-sulfur bonds to carbon-to-hydrogen bonds (C-X C-O C-N C-S to C-H) elimination of halogens (X2) elimination of hydrogen halides (HX) dehydration halomethyl groups to methyl groups (-CH2X to -CH3) aldehyde groups to methyl groups (-CHO to -CH3)

. . Isomerisation (migration of double bonds)

. Formation or cutting of carbon-to-carbon bonds (C-C)

AC21

AC22

AC23

AC24

AC25

AC26

AC27

AC28

AC29

AC30

. . Addition (addition of carbon monoxide (CO) to olefins)

. . Substitution (Wittig reactions)

. . . Carbon-to-hydrogen bonds to carbon-to-carbon bonds (C-H to C-C) (benzene to biphenyl (C6H5C6H5))

. . . Carbon-to-halogen bonds to carbon-to-carbon bonds (C-X to C-C) (condensation by elimination of hydrogen halides (HX))

. . . Carbon-to-oxygen bonds to carbon-to-carbon bonds (C-O to C-C) (dehydration condensation)

. . Decomposition (elimination of carbon dioxide (CO2) or elimination of hydrocarbons)

. . Isomerisation or rearrangement (cis and trans isomerisation or migration of methyl groups)

. . Formation of carbocyclic rings by cyclisation or opening of carbocyclic rings (cyclisation by condensation)

. . Others (metatheses Fischer-Tropsch reactions homologation reactions methyl alcohol or acetone to olefins (CH3OH CH3OCH3 to olefins) disproportionation or transalkylation)

. Halogenation (transhalogenation)

AC40

. Formation or introduction of functional groups containing oxygen

AC41

AC42

AC43

AC44

AC45

AC46

AC47

AC48

AC50

. . Hydroxy groups (OH) or oxy metal groups (O-metal)

. . . Hydroxy groups (OH) or oxy metal groups (O-metal) directly attached to aromatic rings

. . Ether acetal ketal or ortho ester groups

. . Carbonyl groups (-CO)

. . . Aldehyde groups (-CHO)

. . Carboxylic groups (-COOH)

. . . Carboxylic acid salts acid halides or anhydrides

. . Carboxylic acid ester (-COOR) or carbonic ester groups (transesterification)

. Formation or introduction of functional groups containing nitrogen

AC51

AC52

AC53

AC54

AC55

AC56

AC57

AC59

AC60

. . Nitro groups (-NO2) or nitroso groups (-N=O)

. . Amino groups (-NH2) (N-alkylation or quaternisation of amines or N-alkylation of amides)

. . Carboxylic acid amide groups

. . Cyano groups

. . Isocyanate groups (-NCO)

. . Carbamate groups (NH2COO-)

. . Ureido groups (NH2CONH-)

. . Other functional groups containing nitrogen (oxime groups (-NOH) or azo groups (-N=N-))

. Formation or introduction of functional groups containing sulfur (sulfinic acids (RSO2H or sulfuric acid esters (R1R2SO4))

AC61

AC62

AC63

. . Sulfonic acids (RSO3H) or derivatives thereof (sulfonic acid esters or sulfonic acid halides or sulfonamides)

. . Sulfonyl groups (-SO2-) or sulfinyl groups (-SO-) (sulfone (R2SO3) or sulfoxide groups (R2SO))

. . Mercapto groups (-SH) or sulfide groups (-S-)

AC80

. Introduction or elimination of protecting or activating groups

AC81

AC82

AC83

AC84

AC90

. Asymmetric syntheses; Asymmetry holding syntheses

. Racemisation; Complete or partial inversion

. Separation of optically-active compounds; Optical resolution (The subject matter for specific means is also classified in F-terms under viewpoint AD.)

. Introduction of isotopes into organic compounds; Syntheses of labelled compounds

. Other general reactions (preparation of hydrates)

AC91

AC92

AC93

. . Depolymerisation

. . Telomerisation

. . Preparation of inclusion compounds

AD00
PURIFICATION; SEPARATION; STABILISATION; OTHER PHYSICAL TREATMENT

AD10

. Physical treatment

AD11

AD12

AD13

AD14

AD15

AD16

AD17

AD18

AD19

. . Distillation

. . . Azeotropic distillation

. . . Extractive distillation

. . . Steam distillation

. . Crystallisation; Purification or separation of crystals; Crystal precipitation; Granulation

. . Liquid-liquid treatment; Extraction (supercritical or subcritical extraction)

. . Solid-liquid treatment; Solid-gas treatment; Adsorption; Chromatography: Absorption of liquids or gases by solids: Filtration; Decantation: Sublimation

. . Gas-liquid treatment; Condensation; Absorption of gases by liquids

. . Membrane separation (semi-permeable or reverse osmosis membranes)

AD30

. Chemical treatment

AD31

AD32

AD33

AD40

. . using hydrogen

. . Ion exchange

. . by formation of adducts or complexes (separation using inclusion or intermolecular compounds)

. Stabilisation; Use of additives

AD41

. . Polymerisation inhibitors

BA00
ACCELERATION OR SUPPRESSION OF REACTION (THE ART FOR USING REACTION ENGINEERING TECHNIQUES, SEE VIEWPOINT BD)

BA01

BA02

BA03

BA04

BA05

BA06

BA07

BA08

BA09

BA10

. Metal constituents

. . Metals of group 1A i.e. lithium (Li) sodium (Na) potassium (K) rubidium (Rb) caesium (Cs) francium (Fr)

. . . Lithium (Li)

. . . Caesium (Cs)

. . Metals of group 1B i.e. copper Cu) silver (Ag) gold (Au)

. . Metals of group 2A i.e. beryllium (Be) magnesium (Mg) calcium (Ca) strontium (Sr) barium (Ba) radium (Ra)

. . Metals of group 2B i.e. zinc (Zn) cadmium (Cd) mercury (Hg)

. . Metals of group 3A i.e. scandium (Sc) yttrium (Y) lanthanoids actinoids

. . Metals of group 3B i.e. aluminium (Al) gallium (Ga) indium (In) thallium (Tl)

. . Metals of group 4A i.e. titanium (Ti) zirconium (Zr) hafnium (Hf)

BA11

BA12

BA13

BA14

BA15

BA16

BA17

BA18

BA19

BA20

. . Metals of group 4B i.e. germanium (Ge) tin (Sn) lead (Pb)

. . Metals of group 5A i.e. vanadium (V) niobium (Nb) tantalum (Ta)

. . Metals of group 5B i.e. antimony (Sb) bismuth (Bi)

. . Metals of group 6A i.e. chromium (Cr) molybdenum (Mo) tungsten (W)

. . Metals of group 6B i.e. selenium (Se) tellurium (Te) polonium (Po)

. . Metals of group 7A i.e. manganese (Mn) technetium (Tc) rhenium (Re)

. . Metals of group 8

. . . Iron group i.e. iron cobalt nickel

. . . . Iron

. . . . Cobalt

BA21

BA22

BA23

BA24

BA25

BA26

BA27

BA28

BA29

BA30

. . . . Nickel

. . . Platinum group i.e. ruthenium (Ru) rhodium (Rh) palladium (Pd) osmium (Os) iridium (Ir) platinum (Pt)

. . . . Ruthenium

. . . . Rhodium

. . . . Palladium

. . . . Platinum

. Anionic constituents or non-metal constituents

. . Hydrogen (hydrides)

. . Hydroxyl group (hydroxides)

. . Oxygen (oxides)

BA31

BA32

BA33

BA34

BA35

BA36

BA37

BA38

BA39

BA40

. . Boron (borates or borides)

. . Carbon (carbonates carboxylic acid salts alcoholates or AlEt3 (triethylaluminium))

. . Silicon (silicates)

. . Nitrogen (nitrates ammonium salts cyanides NaNH2 (sodium amide) or NaNEt2 (sodium diethylamide))

. . Phosphorus (phosphates or phosphonates)

. . Sulfur (sulfides sulfates sulfonates or thiocyanides)

. . Halogens (halides)

. Coordination constituents

. . Inorganic ligands (halogens)

. . . Carbonyl groups (-CO)

BA41

BA42

BA43

BA44

BA45

BA46

BA47

BA48

BA49

BA50

. . . Amines (NHmRn m=0-3 n=0-3 m+n=3)

. . . Cyano groups (-CN)

. . Organic ligands

. . . Hydrocarbons

. . . Ligands containing oxygen

. . . Ligands containing nitrogen

. . . Ligands having heterocyclic rings

. . . Ligands containing phosphorus

. Organic compound catalysts not containing metals

. . Compounds containing oxygen

BA51

BA52

BA53

BA55

BA56

BA60

. . Compounds containing nitrogen

. . Compounds containing sulfur

. . Compounds containing phosphorus (P) silicon (Si) or boron (B)

. Carrier constituents

. Physical properties of carriers

. Oxidation or dehydrogenation catalysts

BA61

BA62

BA63

BA64

BA65

BA66

BA67

BA68

BA69

BA70

. Reduction or hydrogenation catalysts

. Isomerisation or disproportionation catalysts

. Alkylation or dealkylation catalysts

. Friedel-Crafts catalysts

. Phase transfer catalysts

. Acid catalysts (mineral acids Bronsted acids or protonic acids)

. . Lewis acid catalysts

. . Solid acid catalysts (activated clay or clay minerals)

. Base catalysts

. Raney catalysts

BA71

BA72

BA73

BA74

BA75

BA80

. Zeolites (zeolites aluminosilicates or molecular sieves)

. Ion-exchange resins

. Surfactants

. Alloys (The subject matter is also classified in each constituent.)

. Heteropolyacids (The subject matter is also classified in each constituent.)

. Other features of catalysts

BA81

BA82

BA83

BA84

BA85

BA90

. . Methods of preparation of catalysts (pretreatment or activation)

. . Methods of use (catalyst beds)

. . Methods of recovery or separation

. . Methods of regeneration

. . Physical properties of catalysts

. characterised by the absence of catalysts

BA91

BA92

BA93

BA94

BA95

. Other methods of acceleration or suppression (ultrasonic waves)

. . Acid acceptors (dehydrohalogenation or acid binding agents)

. . Radical initiators

. . Polymerisation inhibitors

. . Light irradiation (actinic rays radiation or sensitising agents)

BB00
REACTION MEDIUM, OR SOLVENT FOR SEPARATION, PURIFICATION OR RECOVERY

BB10

. Organic solvents

BB11

BB12

BB13

BB14

BB15

BB16

BB17

BB18

BB19

BB20

. . Hydrocarbons (naphtha kerosenes petroleum ethers or the like see BB48)

. . Halogenated hydrocarbons

. . Compounds containing oxygen

. . . Alcohols

. . . Ethers

. . . Ketones or aldehydes

. . . Carboxylic acids carboxylic acid esters carbonate esters or carboxylic acid anhydrides

. . Compounds containing nitrogen (nitro compounds)

. . . Amines (NHmRn m=0-3 n=0-3 m+n=3)

. . . Carboxylic acid amides

BB21

BB22

BB23

BB24

BB25

BB26

BB30

. . . Nitriles

. . Compounds containing sulfur

. . Heterocyclic compounds

. . . containing only nitrogen as hetero atoms

. . . containing only oxygen as hetero atoms

. . Compounds containing phosphorus

. . Inorganic solvents

BB31

BB40

. . . Water

. Proticity

BB41

BB42

BB43

BB44

BB45

BB46

BB47

BB48

BB49

. Aproticity (neutral or aprotic)

. Polarity (dipolar solvents)

. Apolarity (non-polarity)

. Acidity

. Basicity

. Water immiscibility (water immiscible or hydrophobic solvents or low-water solubility)

. Water miscibility (aqueous or water-soluble solvents)

. Petroleum-based solvents

. specified by physical representation (boiling point or dielectric constant)

BB60

. Media in gas phase parts

BB61

BB62

BB70

. . Inert gases (nitrogen helium or argon)

. . Water vapours

. characterised by the absence of solvents (absence of organic solvents)

BB71

BB72

. . under anhydrous conditions

. Dissolution aids or emulsifiers

BC00
REACTION PARAMETER

BC10

. Temperatures

BC11

BC12

BC13

BC14

BC15

BC16

BC17

BC18

BC19

. Pressures

. Phases (solid phases)

. . Gas phases

. . Liquid phases

. . . characterised by the conditions of liquid phases (heterogeneous systems or emulsions)

. pH (power of hydrogen) (limitations by numerical values)

. . Acidity

. Velocity (flow rates reflux ratios or space velocity)

. Time

BC30

. Constituent ratios (concentrations of particular constituents)

BC31

BC32

BC33

BC34

BC35

BC36

BC37

BC38

BC40

. . Raw materials/raw materials

. . Catalysts/catalysts

. . Solvents/solvents

. . Raw materials/catalysts

. . Raw materials/solvents

. . Catalysts/solvents

. . Others e.g. limitations of ratios of three or more constituents or limitations of ratios including reaction products

. . mathematising combinations of parameters (special parameters)

. Others (reaction rates conversion rates acid values or ester values)

BC50

. Parameters in separation purification or stabilisation

BC51

BC52

BC53

. . Temperatures

. . Pressures

. . pH (power of hydrogen)

BD00
REACTION ENGINEERING TECHNIQUE

BD10

. Adjustment or treatment of raw material constituents (preheating cooling dilution preliminary purification or phase inversion)

BD20

. Improvement of methods of reactions without depending on improvement of apparatus (removal of particular constituents or reaction heat counter-current reactions or batch types)

BD21

BD30

. . Improvement or control of methods of introduction e.g. divided introduction or specifying the locations of introduction

. Recycling particular constituents or phases e.g. circulation use

BD31

BD32

BD33

BD34

BD35

BD36

BD40

. . Objective compounds

. . Reaction mother liquors i.e. not containing objective compounds as principal constituents

. . . Unreacted raw material constituents or reaction intermediates

. . . Reaction by-products (reaction water)

. . . Solvents

. . . Catalysts

. . Distillation constituents (distillates or bottoms)

BD41

BD42

BD43

BD50

. . Extraction constituents and phase separation constituents (organic phase water phase aqueous flow or aqueous media)

. . Filtration constituents (filtrates)

. . Condensation constituents

. Recycled zones

BD51

BD52

BD53

BD60

. . Raw material feed zones

. . Reaction zones

. . Separation recovery or purification zones

. Multistep treatment of single reaction purification or separation

BD70

. Improvement relating to a plurality of different reactions (use of reaction mixtures resulting from the previous reactions without purification or connections or combinations of processes)

BD80

. Improvement and use of apparatus (use of particular apparatus e.g. tubular reactors vessel type reactors or tray type reactors)

BD81

BD82

BD83

BD84

. . Improvement of the structure of reactors per se

. . Improvement of the structure of separation apparatus or purification apparatus per se

. . Materials (methods of corrosion protection of apparatus)

. . Combinations of apparatus (flow sheets)

BE00
REACTION REAGENT ( CATALYSTS, SEE BA01-BA85)

BE01

BE02

BE03

BE04

BE05

BE06

BE10

. Halides (HX)

. Nitric acid (HNO3) (nitrous acid (HNO2) or hyponitrous acid (H2N2O3))

. Sulfuric acid (H2SO4) (sulfurous acid (H2SO3) oleum or Caro's acid (H2SO5))

. Phosphoric acid (H3PO4) (polyphosphoric acid phosphorous acid (H3PO3) or hypophosphorous acid (HPH2O2))

. Oxyhalogenic acids (HXOn) (perchloric acid (HClO4) periodic acid (HIO4) or hypochlorous acid (HClO))

. Hydrogen cyanide (HCN)

. MOH or M2O(mono-valent metal hydroxides or monovalent metal oxides) (NH4OH (ammonium hydroxide) see BE14)

BE11

BE12

BE13

BE14

BE15

BE20

. M' (OH)2 or M'O (divalent metal hydroxides or divalent oxides)

. M2CO3 (monovalent metal carbonates)

. M'CO3 (divalent metal carbonates)

. Ammonia (NH3)

. MH or M'H2 (monovalent or divalent metal hydrides)

. Hydrogen (H2)

BE21

BE22

BE23

BE24

BE27

BE30

. M or M' (monovalent or divalent metals)

. MAlH4 (monovalent metal aluminium tetrahydrides) or derivatives thereof

. MBH4 (monovalent metal boron tetrahydrides) or derivatives thereof

. M'' (polyvalent metals) (zinc or iron)

. Hydrazine (NH2NH2)

. Oxygen (O2)

BE31

BE32

BE33

BE36

BE40

. Ozone (O3)

. Hydrogen peroxide (H2O2)

. MnO2 (manganese dioxides) CrO3 (chromium trioxide) MMnO4 (metal manganates) M2Cr2O7 (metal dichromates) or MCrO4 (metal chromates)

. MXO2 (halogenites) (potassium hypochlorite (KClO) and sodium periodate (NaIO4)

. Carbon monoxide (CO)

BE41

BE42

BE43

BE44

BE50

. Carbon dioxide (CO2)

. Sulfur dioxide (SO2)

. Sulfur trioxide (SO3)

. Nitrogen dioxide (NO2)

. PX3 (phosphorus trihalides)

BE51

BE52

BE53

BE54

BE55

BE56

BE57

BE60

. SOX2 (thionyl halides) or SO2X2 (sulfuryl halides)

. COX2 (carbonyl halides) (phosgene (COCl2))

. X2 (inter halogen compounds) (iodine monochloride (ICl))

. POX3 (phosphoryl trihalides)

. XSO3H (halogenosulfonic acids)

. BX3 (boron trihalides) (BF3.Et2O (boron trifluoride. ethyl ether complex))

. SX2 (sulfur dihalides)

. Water (H2O)

BE61

BE62

BE63

. MX or M'X2 (monovalent or divalent metal halides)

. M'Xn (polyvalent metal halides)

. M2SO4 or M'SO4 (monovalent or divalent metal sulfates)

BE90

. Others

C07C51/00-66/02;67/00-69/96;213/00-225/36;227/00-229/76;231/00-237/52

BJ00
STRUCTURE OF CARBOCYCLIC RING

BJ10

. Cycloaliphatic groups i.e. rings other than six-membered aromatic rings

BJ20

. . Non-condensed rings

BJ30

. . Condensed rings (condensed rings with six-membered aromatic rings see BJ50)

BJ50

. Six-membered aromatic rings (quinone (O=C6H4=O) rings see BJ10-BJ30)

BM00
HALOGEN

BM10

. CR-X (CR: acyclic carbon)

BM20

. Cy-X (Cy: alicyclic carbon)

BM30

. Ar-X (Ar: aromatic carbon)

BM71

BM72

BM73

BM74

. Fluorine

. Chlorine

. Bromine

. Iodine

BN00
OH (HYDROXY GROUP) OR OM (METAL-OXY GROUP)

BN10

. CR-OH or CR-OM

BN20

. Cy-OH or Cy-OM

BN30

. Ar-OH or Ar-OM

BN90

. OM

BP00
ETHER, ACETAL, KETAL OR ORTHO ESTER

BP10

. CR-O-CR

BP20

. CR-O-Cy

BP30

. CR-O-Ar

BP40

. Cy-O-Cy

BP50

. Cy-O-Ar

BP60

. Ar-O-Ar

BP90

. Acetal ketals or ortho esters

BQ00
ALDEHYDE (RCHO)

BQ10

. CR-CHO

BQ20

. Cy-CHO

BQ30

. Ar-CHO

BR00
KETONE (RR'CO) OR QUINONE (O=C6H4=O)

BR10

. CR-CO-CR

BR20

. CR-CO-Cy

BR30

. CR-CO-Ar

BR40

. Cy-CO-Cy

BR50

. Cy-CO-Ar

BR60

. Ar-CO-Ar

BR70

. with -CO- (carbonyl groups) being part of rings

BR80

. . Quinone rings

BS00
CARBOXYLIC ACID, SALT THEREOF, HALIDE OR ANHYDRIDE

BS10

. CR-COOH CR-COOM CR-COX or (CR-CO)2O

BS20

. Cy-COOH Cy-COOM Cy-COX or (Cy-CO)2O

BS30

. Ar-COOH Ar-COOM Ar-COX or (Ar-CO)2O

BS70

. COOM (carboxylic acid salts)

BS80

. -CO-O-CO- (carboxylic acid anhydrides)

BS85

BS90

. . Mixed acid anhydrides

. -COX (carboxylic acid halides)

C07C213/00-225/36;227/00-229/76;231/00-237/52

BT00
ESTER

BT10

. (CH)-COO-

BT12

BT14

BT16

BT20

. . (CH)-COO-CR

. . (CH)-COO-Cy

. . (CH)-COO-Ar

. Cy-COO-

BT22

BT24

BT26

BT30

. . Cy-COO-CR

. . Cy-COO-Cy

. . Cy-COO-Ar

. Ar-COO-

BT32

BT34

BT36

BT40

. . Ar-COO-CR

. . Ar-COO-Cy

. . Ar-COO-Ar

. Carbonic acid esters (-O-COO-)

BT50

. Haloformic acid esters (-O-COX)

BT60

. Halogen oxyacid esters (-OXn)

BT70

. Nitrites (-O-NO) or nitrates (-O-NO2)

BU00
NITRO, NITROSO OR AMINE

BU10

. -NO (nitroso groups)

BU12

BU14

BU16

BU20

. . CR-NO

. . Cy-NO

. . Ar-NO

. -NO2 (nitro groups)

BU22

BU24

BU26

BU30

. . CR-NO2

. . Cy-NO2

. . Ar-NO2

. -N< (amines) >N+< (quaternary amines) or amino acids

BU32

BU34

BU36

BU38

BU40

. . C-N<

. . . Cy...C-N<

. . . Ar...C-N<

. . . . Ar-C-N<

. . . . Ar-C-C-N<

BU42

BU44

BU46

BU48

BU50

. . Cy-N<

. . . Cy (alicyclic carbon) being condensed rings

. . Ar-N<

. . . Ar (aromatic ring) being condensed

. . >N +< (quaternary ammonium groups)

C07C231/00-237/52

BV00
CARBOXYLIC ACID AMIDE

BV10

. HCON<

BV11

BV12

BV13

BV14

BV15

BV16

BV20

. . Formamide (HCONH2)

. . HCON-CR

. . . Dimethylformamide (HCON(CH3)2 DMF)

. . . Diethylformamide (HCON(C2H5)2)

. . HCON-Cy

. . HCON-Ar

. C-CON< (when carbon is part of acyclic unsaturated hydrocarbons it is classified in BV30-BV37)

BV21

BV22

BV23

BV24

BV25

BV30

. . Acetamide (C-CONH2)

. . C-CON-CR

. . . Dimethylacetamide (CH3CON (CH3)2 DMA)

. . C-CON-Cy

. . C-CON-Ar

. . R' -CON< (R': unsaturated acyclic hydrocarbon groups)

BV31

BV32

BV33

BV34

BV35

BV36

BV37

BV40

. . . R'-CONH2

. . . . Acrylamide (CH2=CHCONH2)

. . . . Methacrylamide (CH2=C(CH3)CONH2)

. . . R'-CON-CR

. . . R'-CON-Cy

. . . R'-CON-Ar

. . . . Acrylanilide (CH2=CHCONHPh)

. . Cy...C-CON<

BV41

BV42

BV43

BV44

BV50

. . . Cy...C-CONH2

. . . Cy...C-CON-CR

. . . Cy...C-CON-Cy

. . . Cy...C-CON-Ar

. . Ar...C-CON<

BV51

BV52

BV53

BV54

BV55

BV60

. . . Ar...C-CONH2

. . . . Phenylacetamide (PhCH2CONH2)

. . . Ar...C-CON-CR

. . . Ar...C-CON-Cy

. . . Ar...C-CON-Ar

. Cy-CON<

BV61

BV62

BV63

BV64

BV70

. . Cy-CONH2

. . Cy-CON-CR

. . Cy-CON-Cy

. . Cy-CON-Ar

. Ar-CON<

BV71

BV72

BV73

BV74

BV80

. . Ar-CONH2

. . Ar-CON-CR

. . Ar-CON-Cy

. . Ar-CON-Ar

. -CON+ (quaternised amide groups) (the subject matter is classified in BV10-BV74)

C07C239/00-239/22;249/04-249/14;251/32-251/70;257/10-259/20;261/00;261/04;269/00-291/06;291/12-291/14

BW00
OXIME

BW10

. H2C=N-O-

BW11

BW12

BW13

BW14

BW15

BW16

BW17

BW18

BW19

BW20

. CR-C=N-O-

. . CR-CH=N-O-

. . CR-C(CR)=N-O-

. Cy-C=N-O-

. . Cy-CH=N-O-

. . Cy-C(CR)=N-O-

. . Cy-C(Cy)=N-O-

. Cy=N-O-

. Ar-C=N-O-

. . Ar-CH=N-O-

BW21

BW22

BW23

BW30

. . Ar-C(CR)=N-O-

. . Ar-C(Cy)=N-O-

. . Ar-C(Ar)=N-O-

. C=N-O-H

BW31

BW32

BW33

BW40

. C=N-O-CR

. C=N-O-Cy

. C=N-O-Ar

. Cy...CR-C=N-O- C=N-O-CR...Cy

BW41

BW42

BW43

BW44

BW45

BW46

. Ar...CR-C=N-O- C=N-O-CR...Ar

. Ar...Cy-C=N-O- C=N-O-Cy...Ar Ar...Cy=N-O-

. with Cy (alicyclic carbon) forming three-membered rings

. with Cy (alicyclic carbon) forming six-membered rings

. with Cy (alicyclic carbon) forming condensed rings

. . with part of condensed rings being aromatic rings

C07B59/00

CN00
TYPE OF ISOTOPE

CN10

. Deuterium

CN20

. Tritium

CN30

. Carbon

CN40

. Halogens

CN50

. . Iodine

CN60

. Other non-metallic elements e.g. boron nitrogen oxygen silicon phosphorus arsenic selenium tellurium or noble gas elements

CN70

. Metallic elements

CN80

. . Group 3A i.e. scandium yttrium lanthanoides or actinoids

CN90

. . Group 7A i.e. manganese technetium or rhenium

C07C1/00-15/62;27/00-39/44

DA00
ZEOLITE, ALUMINOSILICATE; ION-EXCHANGE RESIN

DA10

. Zeolites or aluminosilicates

DA12

DA15

DA20

. . ZSM types (ZSM-5 or ZSM-11)

. . Other than ZSM types (A X Y Nu-1 ferrierite mordenite faujasite or montmorillonite)

. . Compositions (composition ratios)

DA25

DA30

. . . Silica/alumina ratios

. . Acid types or hydrogen types

DA35

DA40

. . Ion exchange or metal ions

. . X-ray diffraction patterns

DA42

DA44

DA46

DA50

. . Constraint coefficients control indexes constraint or constraint indexes (CI)

. . Particle diameters or particle diameter distributions

. . Pore diameters pore volumes or types or sizes of main cavities

. . Processes of preparation raw materials (molar ratios of raw materials see DA20) or reaction reagents and solvents

DA55

DA60

. . Processes of regeneration

. Ion-exchange resins

DA62

DA64

DA66

DA70

. . Acidity e.g.-PO3H2 (phosphoric acids) or -CO2H (carboxylic acids)

. . . Strong acidity e.g. -SO3H (sulfonic acids)

. . Basicity

. . Physical or chemical properties (exchange capacity or average pore diameters)

DA80

. . Processes of preparation or regeneration

C07C17/00-25/28

EA00
HALOGENATED HYDROCARBON

EA01

EA02

EA03

EA10

. Compounds having no rings

. . Saturated compounds

. . Unsaturated compounds

. Compounds having rings

EA11

EA12

EA13

EA14

EA15

EA16

EA17

. . having only rings other than aromatic rings

. . . Saturated compounds

. . . . having two or more rings

. . . . . having condensed rings

. . . Unsaturated compounds

. . . . having two or more rings

. . . . . having condensed rings

EA21

EA22

EA23

. . having only aromatic rings

. . . having two or more rings

. . . . having condensed rings

EA31

EA32

EA33

EA34

EA35

EA36

EA37

EA38

EA39

EA40

. . Having both aromatic rings and other rings than the aromatic rings

. . . all of non-aromatic rings being saturated

. . . . having two rings

. . . . having three rings

. . . . . having one aromatic ring

. . . . . having two aromatic rings

. . . . having four or more rings

. . . at least one of non-aromatic rings being unsaturated

. . . . having two rings

. . . . having three rings

EA41

EA42

EA43

. . . . . having one aromatic ring

. . . . . having two aromatic rings

. . . . having four or more rings

EB00
STABILISER (THE SUBJECT MATTER FOR MIXTURES IS CLASSIFIED IN F-TERMS FOR EACH CONSTITUENT.)

EB01

EB02

EB03

EB04

EB05

EB06

EB07

EB10

. Inorganic compounds

. . Metal compounds

. . . Alumina

. . Non-metal compounds

. . . Silica

. . . Activated carbon

. . Zeolites or other natural inorganic compounds

. Organic compounds

EB11

EB12

EB13

EB14

EB15

EB16

EB17

EB18

EB19

EB20

. . having no heterocyclic rings

. . . Hydrocarbons

. . . Halogenated hydrocarbons

. . . containing oxygen atoms

. . . . having hydroxy group (OH) or metal-oxy groups (O-metal)

. . . . . Saturated compounds

. . . . . Unsaturated compounds

. . . . . . having aromatic rings

. . . . having ether bonds

. . . . . Saturated compounds

EB21

EB22

EB23

EB24

EB25

EB26

EB27

EB28

EB29

EB30

. . . . . Unsaturated compounds

. . . . . . having aromatic rings

. . . . Aldehydes

. . . . Ketones ketenes or quinone

. . . . Carboxylic acids

. . . . Carboxylic acid esters or halogen oxyacid esters

. . . . . Saturated compounds

. . . . . Unsaturated compounds

. . . . . . having aromatic rings

. . . containing nitrogen atoms

EB31

EB32

EB33

EB34

EB35

EB36

EB37

EB38

EB39

EB40

. . . . Nitro nitroso or hydroxyl amino compounds

. . . . . Saturated compounds

. . . . . Unsaturated compounds

. . . . . . having aromatic rings

. . . . having amino groups or quaternary ammonium compounds

. . . . . Saturated compounds

. . . . . Unsaturated compounds

. . . . . . having aromatic rings

. . . . Carboxylic acid amides

. . . . . Saturated compounds

EB41

EB42

EB43

EB44

. . . . . Unsaturated compounds

. . . . . . having aromatic rings

. . . . Carboxylic acid nitriles

. . . containing sulfur atoms

EB51

EB52

EB53

EB54

EB55

EB57

EB58

EB59

EB60

. . having heterocyclic rings

. . . having only nitrogen atoms in heterocyclic rings as hetero atoms

. . . . Substituted or unsubstituted pyridines

. . . . Substituted or unsubstituted pyrimidines

. . . Compounds having only oxygen atoms in heterocyclic rings as hetero atoms

. . . . Substituted or unsubstituted dioxanes

. . . . Substituted or unsubstituted trioxanes

. . . . Epoxy compounds

. . . . . having ether groups

EB61

EB62

EB63

EB64

EB65

. . . . . having ester groups

. . . having only sulfur atoms in heterocyclic rings as hetero atoms

. . . having only nitrogen and oxygen atoms in the same heterocyclic rings as hetero atoms

. . . having only nitrogen and sulfur atoms in the same heterocyclic rings as hetero atoms

. . . having only oxygen and sulfur atoms in the same heterocyclic rings as hetero atoms

EB71

EB72

. . Organic compounds containing elements other than carbon hydrogen halogens oxygen nitrogen and sulfur

. . . containing phosphorus

EB81

EB90

. . Compounds whose structures being unknown or natural organic compounds

. . Organic macromolecular compounds

C07C27/00-39/44

FC00
CARBON SKELETON

FC20

. Cycloaliphatic groups or rings other than six-membered aromatic rings

FC22

FC24

FC26

FC28

FC30

. . Non-condensed rings

. . Condensed rings including spiro condensation (condensed rings with six-membered aromatic rings see FC56)

. . . Condensed rings consisting of two rings

. . . . [3.3.0] systems

. . . . [4.3.0] systems

FC32

FC34

FC36

. . . . [4.4.0] systems

. . . . [2.2.1] systems

. . . Condensed rings consisting of three or more rings

FC50

. Six-membered aromatic rings

FC52

FC54

FC56

. . Non-condensed rings

. . Condensed rings

. . . with non-aromatic rings

FC70

. Unsaturated bonds other than six-membered aromatic rings

FC72

FC74

FC76

FC78

FC80

. . Carbon-to-carbon double bonds (C=C)

. . . One carbon-to-carbon double bond (C=C)

. . . Two carbon-to-carbon double bonds (C=C)

. . . Three or more carbon-to-carbon double bonds (C=C)

. . Carbon-to-carbon triple bonds

FE00
FUNCTIONAL GROUP

FE10

. Hydroxy groups (OH) or metal-oxy groups (OM) (M: metals)

FE11

FE12

FE13

FE19

. . CR-OH or CR-OM (CR: acyclic carbon)

. . Cy-OH or Cy-OM (Cy: alicyclic rings)

. . Ar-OH or Ar-OM (Ar: aromatic rings)

. . Metal-oxy groups (OM ) (also classified in FE11-FE13)

FE70

. Halogens

FE71

FE72

FE73

FE74

FE75

FE76

FE77

. . CR-X

. . Cy-X

. . Ar-X

. . Fluorine

. . Chlorine

. . Bromine

. . Iodine

FG00
ALCOHOL

FG20

. Acyclic aliphatic saturated polyhydric alcohols i.e. not having part of rings or substituents other than hydroxy groups (OH)

FG22

FG24

FG26

FG28

FG29

FG30

. . Dihydric alcohols

. . . Ethylene glycols

. . . Propanediols e.g. 12-13-propanediols

. . . Butanediols e.g. 12-13-14-23-butanediols

. . . Other dihydric alcohols

. . Trihydric alcohols (glycerine)

FG40

. . Tetrahydric alcohols (pentaerythritol)

FG50

. . Pentahydric alcohols (xylitol)

FG60

. . Hexahydric alcohols (sorbitol or mannitol)

FG90

. . Other polyhydric alcohols

C07C41/00-43/32

GN00
PROCESS OF PREPARATION

GN01

GN02

GN03

GN04

GN05

GN06

GN07

GN08

. Formation of ether groups

. . by substitution reactions

. . . from alcohols and halogenated compounds (Williamson syntheses)

. . . from alcohols and ester compounds e.g. dialkyl sulfates aromatic sulfonic acid carboxylic acid esters or phosphate esters

. . . from alcohols and alcohols i.e. dehydration

. . . by opening oxirane rings

. . . by transetherification

. . . by other substitution reactions

GN20

. . by addition reactions

GN21

GN22

GN23

GN24

GN30

. . . Addition to carbon-to-carbon double bonds (C=C)

. . . Addition to carbon-to-carbon triple bonds

. . . Addition to carbonyl (-CO-) compounds

. . Other reactions for forming ether groups

. Formation of acetal (CH3(OCH2H5)2) or ketal (R2C(OR')2) groups

GN31

GN32

GN33

GN34

GN35

GN36

GN37

GN38

. . by substitution reactions

. . . from alcohols and halogen compounds

. . . from alcohols and acetals or thioacetals

. . by addition reactions

. . . Addition to carbon-to-carbon double bonds (C=C)

. . . Addition to carbon-to-carbon triple bonds

. . . Addition to carbonyl (-CO-) compounds

. . by other reactions

GN50

. Formation of ortho ester groups

GN51

GN52

GN53

. . from nitriles

. . from ortho or orthothio esters

. . Other reactions

GP00
OBJECTIVE COMPOUND

GP01

GP02

GP03

GP04

GP05

GP06

GP10

. CR-O-CR (CR: acyclic carbon)

. CR-O-Cy (Cy: alicyclic rings)

. CR-O-Ar (Ar: aromatic rings)

. Cy-O-Cy

. Cy-O-Ar

. Ar-O-Ar

. CR-OH or CR-OM (M: metals)

GP11

GP12

GP20

. Cy-OH or Cy-OM

. Ar-OH or Ar-OM

. CR-X (X: halogens)

GP21

GP22

GP30

. Cy-X

. Ar-X

. Dimethyl ether (CH3OCH3)

GP31

GP40

. Methyl-tertiary-unsubstituted alkyl ethers

. Bisphenol alkylene oxide adduct derivatives

GP41

GP50

. 23 5-Substituted hydroquinone derivatives

. Orthoformic acid esters

GP51

GP52

. Orthoacetic acid esters

. Orthocarbonic acid esters

C07C67/00-69/96

KA00
PROCESS OF PREPARATION OF ESTER

KA01

KA02

KA03

KA04

KA05

KA06

KA10

. Processes of preparation of carboxylic acid esters

. . by reactions of ester groups with each other

. . by reactions between ester groups and hydroxy groups

. . by reactions between carboxylic acids or anhydrides thereof and ester groups (processes of preparation from carboxylic acid halides see KA14)

. . . Ester groups being mineral acid ester groups including compounds having carbon-to-halogen bonds

. . by reactions between carboxylic acids or anhydrides thereof and hydroxy groups (OH) or metal-oxy groups (O-metal) of organic compounds

. . by reactions between carboxylic acids or anhydrides thereof and hydrocarbon groups ( by addition reactions see KA11)

KA11

KA12

KA13

KA14

KA15

KA16

KA17

KA18

KA19

KA20

. . by reactions between carboxylic acids or anhydrides thereof and carbon-to-carbon unsaturated bonds

. . . in the presence of oxygen

. . . . in the presence of platinum group metals or compounds thereof

. . from carboxylic acid halides

. . by conversion of groups containing nitrogen into esters

. . . from amides or lactams

. . . from nitriles

. . by reactions between carboxylic acids or derivatives thereof and carton-to-oxygen ether bonds e.g. acetals or tetrahydrofurans

. . . using oxirane rings

. . from ortho esters

KA30

. . by changing the alcohol moiety of esters without forming ester groups

KA31

KA32

KA33

KA34

KA35

KA36

KA37

. . by changing the acid moiety of esters without forming ester groups

. . by reactions with carbon monoxide or formates (KA02 KA03 KA04 or KA05 takes precedence.)

. . . by reactions between carbon monoxide and ethers

. . . by addition to carbon-to-carbon unsaturated bonds

. . by oxidation of functional groups which change to the acid moiety of esters

. . by oxidation and reduction of aldehydes e.g. Tischenko reactions

. . from ketenes or polyketenes

KA50

. Processes of preparation of carbonic acid esters or haloformic acid esters

KA51

KA52

KA53

KA54

KA55

KA56

KA57

KA58

KA59

KA60

. . Processes of preparation of carbonic acid esters

. . . from phosgene

. . . from haloformates.e.g. from chloroformic acid esters

. . . from carbon dioxide

. . . from inorganic carbonates (from alkali metal carbonate salts)

. . . from carbon dioxide and inorganic carbonates

. . . from organic carbonates

. . . . from alkylene carbonates

. . . from carbon monoxide

. . . . from carbon monoxide and oxygen

KA61

KA62

KA63

KA70

. . . from carbamate esters i.e. urethanes

. . . from ureas

. . . from other compounds

. . Processes of preparation of haloformic acid esters

KA71

KA72

KA73

KA74

. . . from phosgene

. . . from haloformates

. . . from carbon monoxide

. . . from other compounds

C07C69/003-69/017

KC00
ESTER WHEREIN ACID MOIETY CAN TAKE DIFFERENT FORM

KC10

. having esterified carboxylic groups bound to acyclic carbon atoms or hydrogen

KC12

KC14

KC20

. . Saturated carboxylic acid esters

. . Unsaturated carboxylic acid esters

. having esterified carboxylic groups bound to carbon atoms of rings other than six-membered aromatic rings

KC30

. having esterified carboxylic groups bound to carbon atoms of six-membered aromatic rings

C07C69/025

KD00
ALCOHOL MOIETY BEING UNSATURATED ALCOHOL BOUND TO ACYCLIC CARBON ATOM

KD10

. with unsaturated alcohol moiety containing rings

C07C69/54

KE00
ACRYLIC OR METHACRYLIC ACID ESTER

KE10

. using a plurality of polycarboxylic acids as carboxylic acids

KE20

. having esterified hydroxy groups bound to rings

C07C69/66-69/738

KF00
CARBOXYLIC ACID ESTER HAVING SUBSTITUENT CONTAINING OXYGEN

KF10

. having fluorine atoms in carbon chains to which the carbon of esters are bound

KF20

. characterised by the structures of acid moiety

KF21

KF22

KF23

KF24

. . containing cyclopentane or cyclopentene rings

. . containing bicyclooctane or bicyclooctene rings

. . containing Ph-O-Ph (C6H5-O-C6H5) structures

. . containing Ph-C-Ph (C6H5-C-C6H5) structures

C07C227/00-229/76

NB00
AMINO CARBOXYLIC ACID

NB10

. Aspartic acids (Asp)

NB11

NB12

NB13

NB14

NB15

NB16

NB17

NB18

NB19

NB20

. Alanine (Ala)

. Beta-alanine

. Isoleucine (Ile)

. Ornithine (Orn)

. Carnitine

. Glycin (Gly)

. Glutamic acids (Glu)

. Threonine (Thr)

. Serine (Ser)

. Tyrosine (Tyr)

NB21

NB22

NB23

NB24

NB25

NB26

NB27

NB28

. Valine (Val)

. Phenyl alanine (Phe)

. Lysine (Lys)

. Leusine (Leu)

. 34-Dihydroxyphenylalanine (DOPA)

. Ethylene diamine tetraacetic acid (EDTA)

. Iminodiacetic acid

. Nitrilotriacetic acid

C07C253/00-255/67;261/02

QN00
PROCESS OF PREPARATION OF NITRILE

QN02

QN04

QN06

QN08

QN10

. by reactions between nitrogen oxides and organic compounds

. by reactions between cyanogen halides e.g. cyanogen chloride (ClCN) and organic compounds

. from N-formylated amino compounds

. by addition of hydrogen cyanide or salts thereof to unsaturated compounds

. . Addition to carbon-to-carbon double bonds (C=C)

QN12

QN14

QN16

QN18

QN20

. . Addition to carbon-to-carbon triple bonds

. Substitution of cyano groups for halogen atoms

. by reactions between cyanides and lactones or compounds containing etherified or esterified hydroxy groups

. by reactions between ammonia or amines and compounds containing carbon-to-carbon multiple bonds other than six-membered aromatic rings

. by dehydration of carboxylic acid amides

QN22

QN24

QN26

QN28

QN30

. Substitution of cyano groups for carboxyl groups

. Ammoxidation of hydrocarbons

. . containing carbon-to-carbon multiple bonds (unsaturated aldehydes)

. . containing six-membered aromatic rings (styrenes )

. Reactions not involving formation of cyano groups

QN32

. . by dimerisation of cyano compounds

C07C239/00-239/22;249/04-249/14;251/32-251/70;257/10-259/20;261/00;261/04;269/00-291/06;291/12-291/14

RA00
STRUCTURE OF CARBAMIC ACID ESTER

RA02

RA04

RA06

RA08

RA10

. with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms

. . having oxygen atoms of carbamate groups bound to acyclic carbon atoms

. . . to carbon atoms of unsubstituted hydrocarbon groups

. . . to carbon atoms of hydrocarbon groups substituted by halogen atoms or by nitro or nitroso groups

. . . to carbon atoms of hydrocarbon groups substituted by singly-bound oxygen atoms

RA12

RA14

RA16

RA18

RA20

. . . to carbon atoms of oxygen-substituted hydrocarbon groups

. . . to carbon atoms of hydrocarbon groups substituted by nitrogen atoms not being part of nitro or nitroso groups

. . . to carbon atoms of hydrocarbon groups substituted by carboxyl groups

. . having the oxygen atom of at least one of the carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings

. . having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings

RA22

RA24

RA26

RA28

RA30

. . . to carbon atoms of non-condensed six-membered aromatic rings

. . . to carbon atoms of six-membered aromatic rings being part of condensed ring systems

. having nitrogen of carbamate groups bound to carbon of alicyclic rings

. . having oxygen atoms of carbamate groups bound to acyclic carbon atoms

. . having the oxygen atom of at least one of the carbamate groups bound to carbon of alicyclic rings

RA32

RA34

RA36

RA38

RA40

. . having the oxygen atom of at least one of the carbamate groups bound to carbon atoms of six-membered aromatic rings

. having nitrogen atoms of carbamate groups bound to carbon atoms of rings of six-membered aromatic rings

. . having oxygen atoms of carbamate groups bound to acyclic carbon atoms

. . . to carbon atoms of unsubstituted hydrocarbon groups

. . . Halogens (X) nitro or nitroso groups-substituted hydrocarbon groups

RA42

RA44

RA46

RA48

RA50

. . . to carbon atoms of hydrocarbon groups substituted by singly-bound oxygen atoms

. . . to carbon atoms of oxygen-substituted hydrocarbon groups

. . . to carbon atoms of hydrocarbon groups substituted by nitrogen atoms not being part of nitro or nitroso groups

. . . to carbon atoms of hydrocarbon groups substituted by carboxyl groups

. . having oxygen of carbamate groups bound to carbon of alicyclic rings

RA52

RA54

RA56

. . having oxygen of carbamate groups bound to carbon of six-membered aromatic rings

. having two carbamate groups in one molecule

. having three or more carbamate groups in one molecule (for RA54 or RA56 the subject matter is further classified in RA02-RA52 depending on the types of carbon atoms bound to nitrogen or oxygen atoms of carbamate groups.)

RB00
PREPARATION OF CARBAMIC ACID ESTER

RB02

RB04

RB06

RB08

RB10

. using compounds containing nitrogen as raw materials

. . Reactions between amines or ammonia (NH3) and carbonic acid derivatives

. . Reactions between cyanogen halides (XCN) or hydrogen isocyanates (HNCO) and R alcohols (ROH)

. . Reactions between cyanic acid salts and alcohols (ROH) in the presence of acids

. . Reactions between ureas or substituted ureas and alcohols (ROH)

RB12

RB14

RB16

RB18

RB20

. . Reactions between ureas or substituted ureas and epoxides

. . Reaction systems including compounds containing nitrogen carbon monoxide (CO) and alcohols (ROH)

. . . Compounds containing nitrogen being nitro compounds

. . . Compounds containing nitrogen being amines

. . . Compounds containing nitrogen being ureas or substituted ureas

RB22

RB24

RB26

RB28

RB30

. . . with compounds containing nitrogen including two or more kinds of nitro compounds amines and ureas or substituted ureas

. . . including other compounds containing nitrogen

. . using isocyanates i.e. compounds containing -NCO as raw materials

. . . Reactions between isocyanates and alcohols (ROH)

. . . Methods of blocking isocyanates

RB32

RB34

RB36

. . Esterification of carbamic acids or derivatives thereof

. by reactions not involving formation of carbamate groups

. . Methods of methylenation

C07C313/00-323/67

TA00
TYPE OF OBJECTIVE COMPOUND

TA01

TA02

TA03

TA04

TA05

. relating to sulfinyl groups (-SO-)

. relating to sulfonyl groups (-SO2-)

. with sulfinyl groups (-SO-) and sulfonyl groups (-SO2-) being alternative

. relating to sulfide groups (-S-)

. with sulfide groups (-S-) and sulfinyl groups (-SO-) or sulfonyl groups (-SO2-) being alternative

TB00
STRUCTURE OF PARTICULAR PART CONTAINING SULFOXY GROUP (-SON-)

TB01

TB02

TB03

TB04

TB05

. Compounds having particular sulfonyl groups

. . CH3-SO2-

. . CF3-SO2-

. . C6H5-SO2-

. . CH3-C6H4-SO2-

TB11

TB12

TB13

TB14

. Ph-SOn-Ph

. . Ph-SO-Ph

. . Ph-SO2-Ph

. . Ph-S-Ph

TB21

TB22

TB23

. -SOn-C=C<

. . -SOn-CH=CH2

. . . Ar-SOn-CH=CH2

TB31

TB32

TB33

TB34

TB35

TB36

TB37

TB38

TB39

TB40

. -SOn-carbon skeleton-O-

. . -SOn- C...C-O-

. . . -SOn-C-O-

. . . . -SOn-CH2O-

. . . -SOn-C-C-O-

. . . . -SOn-CH2CH2O-

. . . . . Ar-SOn-CH2CH2O-

. . . -SOn-C-C-C-O-

. . -SOn-C...Ar-O-

. . -SOn-Ar...C-O-

TB41

TB42

. . -SOn-Ar...Ar-O-

. . . -SOn-Ar-O-

TB51

TB52

TB53

TB54

TB55

TB56

TB57

TB58

TB59

TB60

. -SOn-carbon skeleton-[COOH]

. . -SOn-C...C-[COOH]

. . . -SOn-C-[COOH]

. . . . -SOn-CH2-[COOH]

. . . -SOn-C-C-[COOH]

. . . . -SOn-CH2CH2-[COOH]

. . -SOn-C...Ar-[COOH]

. . -SOn-Ar...C-[COOH]

. . . -SOn-Ar-C-[COOH]

. . -SOn-Ar...Ar-[COOH]

TB61

. . . -SOn-Ar-[COOH]

TB71

TB72

TB73

TB74

TB75

TB76

TB77

TB78

TB79

TB80

. -S-carbon skeleton-[S]-

. . -S-carbon skeleton-S-

. . . -S-C...C-S-

. . . . -S-C-S-

. . . . -S-C-C-S-

. . . . . -S-CH2CH2-S-

. . -S-carbon skeleton-SO(2)-R

. . . -S-C...C-SO(2)-R

. . . . -S-C-SO(2)-R

. . . -S-Ar...Ar-SO(2)-R

TB81

. . . . -S-Ar-SO(2)-R

TC00
STRUCTURE OF PARTICULAR PART NOT CONTAINING SULFOXY GROUP (-SON-)

TC01

TC02

TC03

TC04

TC05

TC06

TC07

TC08

TC09

TC10

. Saturated or unsaturated non-aromatic carbocyclic ring compounds

. . Saturated or unsaturated three-membered rings

. . . (Three-membered ring)-C-O-

. . . (Three-membered ring)-[COOH]

. . . . >C=C-(three-membered ring)-[COOH]

. . Saturated or unsaturated five-membered rings

. . . Cyclopentanone rings

. . . Cyclopentenone rings

. . Saturated or unsaturated six-membered rings

. . . Saturated or unsaturated cyclohexanone rings

TC11

. . Condensed rings

TC21

TC22

TC23

TC24

TC25

. Ph-X-Ph wherein X is carbon oxygen or nitrogen

. . Ph-C-Ph

. . . Ph-CH2-Ph (diphenyl methane)

. . Ph-O-Ph (diphenyl ether)

. . Ph-CO-Ph (diphenyl ketone)

TC31

TC32

TC33

TC34

TC35

TC36

TC37

. Particular functional groups

. . Ar-OH

. . - CHO

. . > N-C-[COOH]

. . -[SO3H] -SO2-hetero atom groups

. . . -SO2-O-

. . . -SO2-N<

C07C325/00-381/14

TN00
FUNCTIONAL GROUP OF THIO DERIVATIVE

TN10

. Halogens

TN20

. -NO (nitroso groups) or -NO2 (nitro groups)

TN30

. -OH (hydroxy groups) or -O- (ether groups) (-O-acyl see TN60)

TN40

. -CHO (aldehyde group) or -CO- (carbonyl group) e.g. ketones quinones

TN50

. -N< (amino groups) or =N- (imino groups) (>N-acyl see TN60)

TN60

. -COO- -CON< -CN -C(-N)=N- -C(-O)=N- or carboxylic acids and derivatives thereof

TN90

. Other functional groups containing oxygen and/or nitrogen

C07C401/00

UA00
VITAMIN D COMPOUND

UA10

. having functional groups in cyclohexane rings

UA11

UA12

UA13

UA14

UA20

. . Halogens

. . One hydroxy group (-OH)

. . Two or more hydroxy groups (-OH)

. . Others

. having functional groups in carbon chains between rings and condensed rings

UA30

. having functional groups in condensed rings

UA31

UA32

UA33

UA40

. . Halogens

. . Hydroxy groups (OH)

. . Others

. having functional groups in alkyl chains

UA41

UA42

UA43

UA50

. . Halogens

. . Hydroxy groups (OH)

. . Others

. Other structural features

UA51

UA52

. . Previtamin D derivatives

. . 5 6-Trans forms

C07C403/00-403/24

UC00
CYCLOHEXANE OR CYCLOHEXENE HAVING UNSATURATED SIDE CHAIN INCLUDING FOUR OR MORE CARBON ATOMS

UC10

. Structures of rings

UC11

UC12

UC13

UC20

. . Cyclohexane rings

. . Cyclohexene rings

. . Others

. having functional groups directly bound to rings

UC21

UC22

UC23

. . Hydroxy groups (OH)

. . Keto group (>C=O) forming part of rings (cyclohexanone or cyclohexenone or the like)

. . Others

C07C405/00

UE00
PROSTAGLANDIN COMPOUND

UE10

. having functional groups in carboxylic acid side chains

UE11

UE12

UE13

UE14

UE15

UE16

UE17

UE18

. . -Halogens

. . -OH -OR or -OCOR

. . - CHO or -COR

. . -COOH -COOR or -CON<

. . -N<

. . -S-

. . -Heterocyclic rings

. . Others

UE30

. having functional groups in five-membered rings

UE31

UE32

UE33

UE34

UE35

UE36

UE37

UE38

. . -Halogens

. . -OH -OR or -OCOR

. . - CHO or -COR

. . -COOH -COOR or -CON<

. . -N<

. . -S-

. . -Heterocyclic rings

. . Others

UE50

. having functional groups in alkyl side chains

UE51

UE52

UE53

UE54

UE55

UE56

UE57

UE58

. . -Halogens

. . -OH -OR or -OCOR

. . - CHO or -COR

. . -COOH -COOR or -CON<

. . -N<

. . -S-

. . -Heterocyclic rings

. . Others

4H006	ORGANIC LOW-MOLECULAR-WEIGHT COMPOUNDS AND PREPARATION THEREOF
	C07B31/00 -61/00@Z;63/00-63/04;C07C1/00-409/44