CC1=CC=CC=C1N(CC(=O)NC1=CC(=CC=C1)[N+]([O-])=O)S(=O)(=O)C1=CC=C(Cl)C=C1

InChIKey=UMNDNKVQQMVCBJ-UHFFFAOYSA-N

C21H18ClN3O5S

459.9

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonamides Anilides Benzenesulfonyl compounds Nitrobenzenes N-arylamides Nitroaromatic compounds Toluenes Chlorobenzenes Organosulfonamides Aryl chlorides Aminosulfonyl compounds Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic oxides Organochlorides Hydrocarbon derivatives Carbonyl compounds Organic salts Organic cations

Aromatic homomonocyclic compounds

Alpha-amino acid or derivatives - Sulfanilide - Benzenesulfonamide - Nitrobenzene - Anilide - Benzenesulfonyl group - N-arylamide - Nitroaromatic compound - Halobenzene - Toluene - Chlorobenzene - Aryl chloride - Organosulfonic acid amide - Aryl halide - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Carboxamide group - Organic nitro compound - C-nitro compound - Secondary carboxylic acid amide - Allyl-type 1,3-dipolar organic compound - Propargyl-type 1,3-dipolar organic compound - Carboxylic acid derivative - Organic 1,3-dipolar compound - Organic oxoazanium - Organosulfur compound - Organooxygen compound - Organohalogen compound - Organochloride - Organic oxygen compound - Organic salt - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic cation - 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