COC1=CC=C(C=C1)S(=O)(=O)N(CC1=CC=C(C=C1)[N+]([O-])=O)C1=C(C=CC=C1C)C(=O)NO

InChIKey=XXPSBHJSGLKGLL-UHFFFAOYSA-N

C22H21N3O7S

471.48

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides m-Toluamides Benzenesulfonyl compounds Benzoic acids and derivatives Nitrobenzenes Phenoxy compounds Anisoles Nitroaromatic compounds Methoxybenzenes Benzoyl derivatives Alkyl aryl ethers Organosulfonamides Vinylogous amides Aminosulfonyl compounds Hydroxamic acids Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Organonitrogen compounds Organic oxides Organic salts Organic zwitterions Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - M-toluamide - Toluamide - Benzoic acid or derivatives - Nitrobenzene - Phenoxy compound - Nitroaromatic compound - Anisole - Benzoyl - Methoxybenzene - Phenol ether - Alkyl aryl ether - Toluene - Organosulfonic acid amide - Vinylogous amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Organic nitro compound - Hydroxamic acid - C-nitro compound - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Ether - Organic 1,3-dipolar compound - Organic oxoazanium - Hydrocarbon derivative - Organic oxygen compound - Organic oxide - Organic zwitterion - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic salt - 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