CC([O-])=O.CCN(CC[N+]1=CC=CC=C1)C1=CC=C(C=C1)N=NC1=C(Cl)C=C(C=C1)[N+]([O-])=O

InChIKey=WQIDMVKHMHGZPN-UHFFFAOYSA-M

C23H24ClN5O4

469.93

Organic compounds

Organoheterocyclic compounds

Azobenzenes

Not available

Not available

Azobenzenes

Nitrobenzenes Aniline and substituted anilines Dialkylarylamines Nitroaromatic compounds Chlorobenzenes Pyridinium derivatives Aryl chlorides Heteroaromatic compounds Azo compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboxylic acids Organic oxoazanium compounds Monocarboxylic acids and derivatives Organochlorides Organic salts Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations

Not available

Azobenzene - Nitrobenzene - Nitroaromatic compound - Tertiary aliphatic/aromatic amine - Dialkylarylamine - Aniline or substituted anilines - Chlorobenzene - Halobenzene - Monocyclic benzene moiety - Pyridine - Pyridinium - Benzenoid - Aryl chloride - Aryl halide - Heteroaromatic compound - C-nitro compound - Organic nitro compound - Tertiary amine - Azo compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Carboxylic acid - Organic oxoazanium - Monocarboxylic acid or derivatives - Azacycle - Hydrocarbon derivative - Organic salt - Organic nitrogen compound - Organohalogen compound - Amine - Organochloride - Organonitrogen compound - Carbonyl group - Organooxygen compound - Organic oxygen compound - Organic oxide - Organic cation - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as azobenzenes. These are organonitrogen aromatic compounds that contain a central azo group, where each nitrogen atom is conjugated to a benzene ring.

Not available