COC1=C(OC)C=C(C=NNC(=O)CN(C2=CC=CC=C2)S(=O)(=O)C2=CC=CC=C2[N+]([O-])=O)C=C1

InChIKey=DTYWRTNWJVBPAA-UHFFFAOYSA-N

C23H22N4O7S

498.51

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonamides Dimethoxybenzenes Benzenesulfonyl compounds Nitrobenzenes Anisoles Phenoxy compounds Nitroaromatic compounds Alkyl aryl ethers Organosulfonamides Aminosulfonyl compounds Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic zwitterions Hydrocarbon derivatives Organonitrogen compounds Carbonyl compounds Organic oxides Organic salts

Aromatic homomonocyclic compounds

Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Dimethoxybenzene - O-dimethoxybenzene - Nitrobenzene - Benzenesulfonyl group - Methoxybenzene - Anisole - Phenoxy compound - Phenol ether - Nitroaromatic compound - Alkyl aryl ether - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic nitro compound - C-nitro compound - Carboxylic acid derivative - Ether - Organic 1,3-dipolar compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxide - Organic salt - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Carbonyl group - Organic zwitterion - 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