CC1=C(C=C(Cl)C=C1)N(CC(=O)N1CCN(CC2=CC=CC=C2)CC1)S(=O)(=O)C1=CC=CC=C1

InChIKey=UGNGSALEXJAYHG-UHFFFAOYSA-N

C26H28ClN3O3S

498.04

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Alpha amino acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds Phenylmethylamines Benzylamines Toluenes N-alkylpiperazines Aralkylamines Chlorobenzenes Organosulfonamides Aryl chlorides Tertiary carboxylic acid amides Aminosulfonyl compounds Trialkylamines Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Benzylamine - Phenylmethylamine - Aralkylamine - Chlorobenzene - N-alkylpiperazine - Halobenzene - Toluene - Aryl chloride - Aryl halide - 1,4-diazinane - Piperazine - Organosulfonic acid amide - Aminosulfonyl compound - Tertiary carboxylic acid amide - Sulfonyl - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Amino acid or derivatives - Tertiary amine - Carboxamide group - Tertiary aliphatic amine - Organoheterocyclic compound - Carboxylic acid derivative - Azacycle - Organohalogen compound - Organic nitrogen compound - Organic oxygen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Amine - Organochloride - Organonitrogen compound - Organooxygen compound - Organosulfur compound - 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