CS(=O)(=O)NC1=CC=C(C=C1)C1=CC(N(N1)C(=O)CCC(O)=O)C1=CC(=CC=C1)[N+]([O-])=O

InChIKey=FFHYMUBGSHRMCH-UHFFFAOYSA-N

C20H20N4O7S

460.46

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Nitrobenzenes Nitroaromatic compounds Organosulfonamides Organic sulfonamides Pyrazolines Aminosulfonyl compounds Carboxylic acid hydrazides Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboxylic acids Organic oxoazanium compounds Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Organic salts Organic zwitterions Carbonyl compounds Organonitrogen compounds Organopnictogen compounds

Aromatic heteromonocyclic compounds

Sulfanilide - Nitrobenzene - Nitroaromatic compound - Organic sulfonic acid amide - Organosulfonic acid amide - Pyrazoline - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Aminosulfonyl compound - Carboxylic acid hydrazide - C-nitro compound - Organic nitro compound - Carboxylic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Hydrocarbon derivative - Carbonyl group - Organic salt - Organic oxygen compound - Organopnictogen compound - Organic nitrogen compound - Organic zwitterion - 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