CC1=CC(C)=C(NS(=O)(=O)C2=C(NN=C(CCC(O)=O)C3=CC=CS3)C=CC(=C2)[N+]([O-])=O)C=C1

InChIKey=JJKZSYCFOJWOAB-UHFFFAOYSA-N

C22H22N4O6S2

502.56

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Nitrobenzenes m-Xylenes Phenylhydrazines Nitroaromatic compounds Organosulfonamides Aminosulfonyl compounds Heteroaromatic compounds Thiophenes Organic oxoazanium compounds Monocarboxylic acids and derivatives Hydrazones Carboxylic acids Propargyl-type 1,3-dipolar organic compounds Organic oxides Organic zwitterions Hydrocarbon derivatives Carbonyl compounds Organic salts

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Nitrobenzene - Benzenesulfonyl group - Nitroaromatic compound - Phenylhydrazine - M-xylene - Xylene - Organosulfonic acid amide - Heteroaromatic compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Thiophene - Aminosulfonyl compound - C-nitro compound - Organic nitro compound - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Allyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Carboxylic acid derivative - Carboxylic acid - Hydrazone - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic zwitterion - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organosulfur compound - Organic oxide - Hydrocarbon derivative - Organic nitrogen compound - Carbonyl group - Organic salt - Aromatic heteromonocyclic 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