OS([O-])(=O)=O.CCN(CC[N+]1=CC=CC=C1)C1=CC=C(C=C1)N=NC1=C(Cl)C=C(C=C1Cl)[N+]([O-])=O

InChIKey=WWVHJFVMRCTKCV-UHFFFAOYSA-M

C21H21Cl2N5O6S

542.39

Organic compounds

Organoheterocyclic compounds

Azobenzenes

Not available

Not available

Azobenzenes

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

Aromatic heteromonocyclic compounds

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