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| SECTION C CHEMISTRY; METALLURGY |
| C 07 | ORGANIC CHEMISTRY (such compounds as the oxides, sulfides, or oxysulfides of carbon, cyanogen, phosgene, hydrocyanic acid or salts thereof C01; products obtained from layered base-exchange silicates by ion-exchange with organic compounds such as ammonium, phosphonium or sulfonium compounds or by intercalation of organic compounds C01B 33/44; macromolecular compounds C08; dyes C09; fermentation products C12; fermentation or enzyme-using processes to synthesise a desired chemical compound or composition or to separate optical isomers from a racemic mixture C12P; production of organic compounds by electrolysis or electrophoresis C25B 3/00, C25B 7/00) [2] |
| C 07 C | ACYCLIC OR CARBOCYCLIC COMPOUNDS |
| Notes |
| (1) | In this subclass, the following terms or expressions are used with the meanings indicated: |
| | "bridged" means the presence of at least one fusion other than ortho, peri or spiro; |
| | two rings are "condensed" if they share at least one ring member, i.e. "spiro" and "bridged" are considered as condensed; |
| | "condensed ring system" is a ring system in which all rings are condensed among themselves; |
| | "number of rings" in a condensed ring system equals the number of scissions necessary to convert the ring system into one acyclic chain; |
| | "quinones" are compounds derived from compounds containing a six-membered aromatic ring or a system comprising six-membered aromatic rings (which system may be condensed or not condensed) by replacing two or four |
| (2) | Therapeutic activity of compounds is further classified in subclass A61P. [7] |
| (3) | In this subclass, in the absence of an indication to the contrary, a process is classified in the last appropriate place. [3] |
| (4) | In this subclass, in the absence of an indication to the contrary, "quaternary ammonium compounds" are classified with the corresponding "non-quaternised nitrogen compounds". [5] |
| (5) | For the classification of compounds in groups C07C 1/00 to C07C 71/00 and C07C 401/00 to C07C 409/00 : |
| | a compound is classified considering the molecule as a whole (rule of the "whole molecule approach"); |
| | a compound is considered to be saturated if it does not contain carbon atoms bound to each other by multiple bonds; |
| | a compound is considered to be unsaturated if it contains carbon atoms bound to each other by multiple bonds, which includes a six-membered aromatic ring, |
| unless otherwise specified or implicitly derivable from the subdivision, as in group C07C 69/00, e.g. C07C 69/712. [5] |
| (6) | For the classification of compounds in groups C07C 201/00 to C07C 395/00, i.e. after the functional group has been determined according to the "last place rule", a compound is classified according to the following principles: |
| | compounds are classified in accordance with the nature of the carbon atom to which the functional group is attached; |
| | a carbon skeleton is a carbon atom, other than a carbon atom of a carboxyl group, or a chain of carbon atoms bound to each other; a carbon skeleton is considered to be terminated by every bond to an element other than carbon or to a carbon atom of a carboxyl group; |
| | when the molecule contains several functional groups, only functional groups linked to the same carbon skeleton as the one first determined are considered; |
| | a carbon skeleton is considered to be saturated if it does not contain carbon atoms bound to each other by multiple bonds; |
| | a carbon skeleton is considered to be unsaturated if it contains carbon atoms bound to each other by multiple bonds, which includes a six-membered aromatic ring. [5] |
| (7) | In this subclass, it is desirable to add the indexing codes of subclass C07M. The indexing codes should be unlinked. [6] |
| Subclass Index |
| COMPOUNDS CONTAINING CARBON AND HYDROGEN ONLY |
| Preparation |
| Purification, separation, stabilisation |
| Compounds |
| aliphatic |
| cycloaliphatic, aromatic |
| COMPOUNDS CONTAINING CARBON AND HALOGENS, WITH OR WITHOUT HYDROGEN |
| Preparation |
| Compounds |
| aliphatic |
| cycloaliphatic, aromatic |
| COMPOUNDS CONTAINING CARBON AND OXYGEN, WITH OR WITHOUT HYDROGEN OR HALOGENS |
| Preparation |
| simultaneous production of more than one class of oxygen- containing compounds |
| of alcohols; of phenols |
| of ethers or acetals; of oxo compounds |
| of quinones |
| of carboxylic acids, their salts or anhydrides |
| of esters of carboxylic acids |
| of esters of carbonic or haloformic acids |
| Compounds |
| with OH group(s): aliphatically bound |
| cycloaliphatically bound |
| with OH group(s) aromatically bound |
| Ethers, acetals, orthoesters; aldehydes; ketones |
| Quinones |
| carboxylic acids |
| acyclic |
| cyclic |
| Esters |
| COMPOUNDS CONTAINING CARBON AND NITROGEN, WITH OR WITHOUT HYDROGEN, HALOGENS, OR OXYGEN |
| Preparation |
| of amines |
| of hydroxy amines, aminoethers, or aminoesters |
| of aminoaldehydes, aminoketones, aminoquinones |
| of aminocarboxylic acids |
| of amides of carboxylic acids |
| of nitriles of carboxylic acids |
| of derivatives of hydrazine |
| of compounds containing carbon- to-nitrogen double bonds, e.g. imines, hydrazones, isocyanates |
| of derivatives of carbamic acids |
| of urea or derivatives |
| of guanidines or derivatives |
| of nitro or nitroso compounds, or esters of nitric or nitrous acids |
| Compounds |
| having nitrogen bound to carbon or to carbon and hydrogen |
| Amines |
| Hydroxy amines; Aminoethers; Aminoesters |
| Aminoaldehydes, aminoketones, aminoquinones |
| Amino carboxylic acids |
| Amides of carboxylic acids |
| Compounds containing one or more carbon-to-nitrogen double bonds, e.g. imines |
| Nitriles of carboxylic acids |
| Amidines, imino-ethers |
| Hydroxamic acids |
| Derivatives of cyanic or isocyanic acid |
| Carbodiimides |
| Carbamic acids |
| Ureas |
| Guanidines |
| having nitrogen bound to halogens |
| having nitrogen bound to oxygen |
| Nitro or nitroso compounds |
| Nitrites or nitrates |
| Hydroxylamines |
| Oximes |
| having nitrogen bound to another nitrogen |
| Hydrazines, hydrazides |
| Semicarbazates, semicarbazides |
| Azo compounds, diazo compounds |
| Hydrazones, hydrazidines |
| Semicarbazones |
| N-nitro or N-nitroso compounds |
| containing chains of three nitrogen atoms bound together |
| Triazenes |
| Azides |
| Other compounds containing nitrogen |
| COMPOUNDS CONTAINING CARBON, TOGETHER WITH SULFUR, SELENIUM, OR TELLURIUM, WITH OR WITHOUT HYDROGEN, HALOGENS, OXYGEN, OR NITROGEN |
| Preparation |
| of derivatives of sulfuric or sulfonic acids |
| of mercaptans, thiophenols, sulfides, or polysulfides |
| of sulfones or sulfoxides |
| Compounds |
| having sulfur bound to oxygen |
| Esters of sulfurous or sulfuric acids |
| Sulfonic acids or derivatives |
| Sulfenic or sulfinic acids or derivatives |
| Sulfones, sulfoxides |
| having sulfur bound to carbon |
| Mercaptans, thiophenols, sulfides or polysulfides |
| Thioaldehydes, thioketones |
| Thiocarboxylic acids or derivatives |
| Thiocarbonic acids or derivatives |
| Thiocyanates, isothiocyanates |
| Thiocarbamic acids or derivatives |
| Thioureas |
| Thiosemicarbazides or thiosemicarbazones |
| having sulfur bound to nitrogen |
| Sulfonamides |
| Sulfenamides, sulfinamides, sulfenylcarbamates or sulfenylureas |
| Amides of sulfuric acids |
| Other compounds containing sulfur |
| Compounds containing selenium |
| Compounds containing tellurium |
| IRRADIATION PRODUCTS OF CHOLESTEROL |
| DERIVATIVES OF CYCLOHEXANE OR OF A CYCLOHEXENE HAVING AN UNSATURATED SIDE-CHAIN WITH AT LEAST FOUR CARBON ATOMS |
| PROSTAGLANDINS OR DERIVATIVES |
| PEROXIDES; PEROXYACIDS |
| Preparation |
| Compounds |
| Hydrocarbons (derivatives of cyclohexane or of a cyclohexene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene rings C07C 403/00; preparation of macromolecular compounds C08; production or separation from undefined hydrocarbon mixtures such as petroleum oil C10G; natural gas, synthetic natural gas, liquefied petroleum gas C10L 3/00; electrolytic or electrophoretic processes C25B) [3] |
1/ | 00 | Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon |
1/ | 02 | . | from oxides of carbon (preparation of liquid hydrocarbon mixtures of undefined composition C10G 2/00; of synthetic natural gas C10L 3/06) [5] |
1/ | 04 | . | . | from carbon monoxide with hydrogen |
1/ | 06 | . | . | . | in the presence of organic compounds, e.g. hydrocarbons |
1/ | 08 | . | . | . | Isosyntheses |
1/ | 10 | . | . | from carbon monoxide with water vapour |
1/ | 12 | . | . | from carbon dioxide with hydrogen |
1/ | 20 | . | starting from organic compounds containing only oxygen atoms as hetero atoms |
1/ | 207 | . | . | from carbonyl compounds [5] |
1/ | 213 | . | . | . | by splitting of esters [5] |
1/ | 22 | . | . | by reduction |
1/ | 24 | . | . | by elimination of water |
1/ | 247 | . | . | by splitting of cyclic ethers [3] |
1/ | 26 | . | starting from organic compounds containing only halogen atoms as hetero atoms |
1/ | 28 | . | . | by ring closure |
1/ | 30 | . | . | by splitting-off the elements of hydrogen halide from a single molecule |
1/ | 32 | . | starting from compounds containing hetero atoms other than, or in addition to, oxygen or halogen [3] |
1/ | 34 | . | . | reacting phosphines with aldehydes or ketones, e.g. Wittig reaction [3] |
1/ | 36 | . | by splitting of esters (C07C 1/213, C07C 1/30 take precedence) [3,5] |
2/ | 00 | Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms (redistribution reactions involving splitting C07C 6/00) [3] |
2/ | 02 | . | by addition between unsaturated hydrocarbons [3] |
2/ | 04 | . | . | by oligomerisation of well-defined unsaturated hydrocarbons without ring formation [3] |
2/ | 06 | . | . | . | of alkenes, i.e. acyclic hydrocarbons having only one carbon-to-carbon double bond [3] |
2/ | 08 | . | . | . | . | Catalytic processes [3] |
2/ | 10 | . | . | . | . | . | with metal oxides [3] |
2/ | 12 | . | . | . | . | . | with crystalline alumino-silicates, e.g. molecular sieves [3] |
2/ | 14 | . | . | . | . | . | with inorganic acids; with salts or anhydrides of acids [3] |
2/ | 16 | . | . | . | . | . | . | Acids of sulfur; Salts thereof; Sulfur oxides [3] |
2/ | 18 | . | . | . | . | . | . | Acids of phosphorus; Salts thereof; Phosphorus oxides [3] |
2/ | 20 | . | . | . | . | . | . | Acids of halogen; Salts thereof [3] |
2/ | 22 | . | . | . | . | . | . | . | Metal halides; Complexes thereof with organic compounds [3] |
2/ | 24 | . | . | . | . | . | with metals [3] |
2/ | 26 | . | . | . | . | . | with hydrides or organic compounds (C07C 2/22 takes precedence) [3] |
2/ | 28 | . | . | . | . | . | . | with ion-exchange resins [3] |
2/ | 30 | . | . | . | . | . | . | containing a metal-to-carbon bond; Metal hydrides [3] |
2/ | 32 | . | . | . | . | . | . | as complexes, e.g. acetyl-acetonates [3] |
2/ | 34 | . | . | . | . | . | . | . | Metal-hydrocarbon complexes [3] |
2/ | 36 | . | . | . | . | . | . | as phosphines, arsines, stilbines or bismuthines [3] |
2/ | 38 | . | . | . | of dienes or alkynes [3] |
2/ | 40 | . | . | . | . | of conjugated dienes [3] |
2/ | 42 | . | . | homo- or co-oligomerisation with ring formation, not being a Diels-Alder conversion [3] |
2/ | 44 | . | . | . | of conjugated dienes only [3] |
2/ | 46 | . | . | . | . | Catalytic processes [3] |
2/ | 48 | . | . | . | of only hydrocarbons containing a carbon-to-carbon triple bond [3] |
2/ | 50 | . | . | Diels-Alder conversion [3] |
2/ | 52 | . | . | . | Catalytic processes [3] |
2/ | 54 | . | by addition of unsaturated hydrocarbons to saturated hydrocarbons, or to hydrocarbons containing a six-membered aromatic ring with no unsaturation outside the aromatic ring [3] |
2/ | 56 | . | . | Addition to acyclic hydrocarbons [3] |
2/ | 58 | . | . | . | Catalytic processes [3] |
2/ | 60 | . | . | . | . | with halides [3] |
2/ | 62 | . | . | . | . | with acids [3] |
2/ | 64 | . | . | Addition to a carbon atom of a six-membered aromatic ring [3] |
2/ | 66 | . | . | . | Catalytic processes [3] |
2/ | 68 | . | . | . | . | with halides [3] |
2/ | 70 | . | . | . | . | with acids [3] |
2/ | 72 | . | . | Addition to a non-aromatic carbon atom of hydrocarbons containing a six-membered aromatic ring [3] |
2/ | 74 | . | by addition with simultaneous hydrogenation [3] |
2/ | 76 | . | by condensation of hydrocarbons with partial elimination of hydrogen [3] |
2/ | 78 | . | . | Processes with partial combustion [3] |
2/ | 80 | . | . | Processes with the aid of electrical means [3] |
2/ | 82 | . | . | oxidative coupling [3] |
2/ | 84 | . | . | . | catalytic [3] |
2/ | 86 | . | by condensation between a hydrocarbon and a non-hydrocarbon [3] |
2/ | 88 | . | . | Growth and elimination reactions (preparation of metallo-organic compounds C07F) [3] |
4/ | 00 | Preparation of hydrocarbons from hydrocarbons containing a larger number of carbon atoms (redistribution reactions involving splitting C07C 6/00; cracking hydrocarbon oils C10G) [3] |
4/ | 02 | . | by cracking a single hydrocarbon or a mixture of individually defined hydrocarbons or a normally gaseous hydrocarbon fraction [3] |
4/ | 04 | . | . | Thermal processes [3] |
4/ | 06 | . | . | Catalytic processes [3] |
4/ | 08 | . | by splitting-off an aliphatic or cycloaliphatic part from the molecule [3] |
4/ | 10 | . | . | from acyclic hydrocarbons [3] |
4/ | 12 | . | . | from hydrocarbons containing a six-membered aromatic ring, e.g. propyltoluene to vinyltoluene [3] |
4/ | 14 | . | . | . | splitting taking place at an aromatic-aliphatic bond [3] |
4/ | 16 | . | . | . | . | Thermal processes [3] |
4/ | 18 | . | . | . | . | Catalytic processes [3] |
4/ | 20 | . | . | . | . | Hydrogen being formed in situ, e.g. from steam [3] |
4/ | 22 | . | by depolymerisation to the original monomer, e.g. dicyclopentadiene to cyclopentadiene [3] |
4/ | 24 | . | by splitting polyarylsubstituted aliphatic compounds at an aliphatic-aliphatic bond, e.g. 1,4-diphenylbutane to styrene [3] |
4/ | 26 | . | by splitting polyaryl compounds at a bond between uncondensed six-membered aromatic rings, e.g. biphenyl to benzene [3] |
5/ | 00 | Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms |
5/ | 02 | . | by hydrogenation (simultaneous hydrogenation and dehydrogenation C07C 5/52) |
5/ | 03 | . | . | of non-aromatic carbon-to-carbon double bonds [3] |
5/ | 05 | . | . | . | Partial hydrogenation [3] |
5/ | 08 | . | . | of carbon-to-carbon triple bonds |
5/ | 09 | . | . | . | to carbon-to-carbon double bonds [3] |
5/ | 10 | . | . | of aromatic six-membered rings |
5/ | 11 | . | . | . | Partial hydrogenation [3] |
5/ | 13 | . | . | with simultaneous isomerisation [3] |
5/ | 22 | . | by isomerisation (with simultaneous hydrogenation C07C 5/13; with simultaneous dehydrogenation C07C 5/373) |
5/ | 23 | . | . | Rearrangement of carbon-to-carbon unsaturated bonds [3] |
5/ | 25 | . | . | . | Migration of carbon-to-carbon double bonds [3] |
5/ | 27 | . | . | Rearrangement of carbon atoms in the hydrocarbon skeleton [3] |
5/ | 29 | . | . | . | changing the number of carbon atoms in a ring while maintaining the number of rings [3] |
5/ | 31 | . | . | . | changing the number of rings [3] |
5/ | 32 | . | by dehydrogenation with formation of free hydrogen [2] |
5/ | 327 | . | . | Formation of non-aromatic carbon-to-carbon double bonds only [3] |
5/ | 333 | . | . | . | Catalytic processes [3] |
5/ | 35 | . | . | Formation of carbon-to-carbon triple bonds only [3] |
5/ | 367 | . | . | Formation of an aromatic six-membered ring from an existing six-membered ring, e.g. dehydrogenation of ethylcyclohexane to ethylbenzene [3] |
5/ | 373 | . | . | with simultaneous isomerisation [3] |
5/ | 387 | . | . | . | of cyclic compounds containing no six-membered ring to compounds containing a six-membered aromatic ring [3] |
5/ | 393 | . | . | . | with cyclisation to an aromatic six-membered ring, e.g. dehydrogenation of n-hexane to benzene [3] |
5/ | 41 | . | . | . | . | Catalytic processes [3] |
5/ | 42 | . | by dehydrogenation with a hydrogen acceptor [2] |
| Notes |
| (1) | In this group: |
| | the catalyst is considered as forming part of the acceptor system in case of simultaneous catalyst reduction; [3] |
| | compounds added for binding the reduced acceptor system are not considered as belonging to the acceptor system. [3] |
| (2) | The acceptor system is classified according to the supplying substances in case of in situ formation of the acceptor system or of in situ regeneration of the reduced acceptor system. [3] |
5/ | 44 | . | . | with a halogen or a halogen-containing compound as an acceptor [2] |
5/ | 46 | . | . | with sulfur or a sulfur-containing compound as an acceptor [2] |
5/ | 48 | . | . | with oxygen as an acceptor [2] |
5/ | 50 | . | . | with an organic compound as an acceptor [2] |
5/ | 52 | . | . | . | with a hydrocarbon as an acceptor, e.g. hydrocarbon disproportionation, i.e. 2 CnHp |
5/ | 54 | . | . | with an acceptor system containing at least two compounds provided for in more than one of groups C07C 5/44 to C07C 5/50 [3] |
5/ | 56 | . | . | . | containing only oxygen and either halogens or halogen-containing compounds [3] |
| C07C 6/00 - C07C 13/72 |