CCOC1=CC=CC=C1\C=N\NC1=C(C=C(C=C1)[N+]([O-])=O)S(=O)(=O)NC1=CC=CC=C1Cl

InChIKey=QJNUXOHWMGCNTB-OEAKJJBVSA-N

C21H19ClN4O5S

474.92

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes Phenylhydrazines Phenoxy compounds Phenol ethers Nitroaromatic compounds Alkyl aryl ethers Chlorobenzenes Aryl chlorides Organosulfonamides Aminosulfonyl compounds Hydrazones Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic salts Hydrocarbon derivatives Organic zwitterions Organochlorides Organic oxides

Aromatic homomonocyclic compounds

Sulfanilide - Benzenesulfonamide - Benzenesulfonyl group - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Phenylhydrazine - Phenol ether - Alkyl aryl ether - Chlorobenzene - Halobenzene - Organosulfonic acid amide - Aryl chloride - Aryl halide - Sulfonyl - Aminosulfonyl compound - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Organic nitro compound - C-nitro compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Ether - Hydrazone - Organic 1,3-dipolar compound - Organic oxoazanium - Organic zwitterion - Organohalogen compound - Organochloride - Organonitrogen compound - Organic salt - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organosulfur compound - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

Not available