CC(C)C1=CC2=C(NNC3=C(C=C(C=C3)S(=O)(=O)NC3=C(C)C=C(C)C=C3)[N+]([O-])=O)C(=O)N=C2C=C1

InChIKey=WISDFGRFNYHVHW-UHFFFAOYSA-N

C25H25N5O5S

507.57

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonamides Nitrobenzenes Indoles and derivatives Benzenesulfonyl compounds Cumenes m-Xylenes Phenylhydrazines Nitroaromatic compounds Organosulfonamides Aminosulfonyl compounds N-acylimines Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Azacyclic compounds Carbonyl compounds Hydrazines and derivatives Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions

Aromatic heteropolycyclic compounds

Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Cumene - Benzenesulfonyl group - Indole or derivatives - Nitrobenzene - Nitroaromatic compound - M-xylene - Xylene - Phenylhydrazine - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - N-acylimine - C-nitro compound - Organic nitro compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organic oxoazanium - Carbonyl group - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Hydrazine derivative - Organic oxide - Organic zwitterion - Organic salt - Organic oxygen compound - Aromatic heteropolycyclic 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