Cl.CN1CCN(CC1)NC(=O)C1=CC(=C(Cl)C=C1)S(=O)(=O)NC1=CC=C(Cl)C=C1

InChIKey=YBWJWHWUQVHQHF-UHFFFAOYSA-N

C18H21Cl3N4O3S

479.8

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

4-halobenzoic acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds Benzoyl derivatives N-methylpiperazines Chlorobenzenes Organosulfonamides Aryl chlorides Aminosulfonyl compounds Trialkylamines Amino acids and derivatives Carboxylic acid hydrazides Azacyclic compounds Organooxygen compounds Hydrochlorides Organic oxides Organochlorides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Halobenzoic acid or derivatives - 4-halobenzoic acid or derivatives - Sulfanilide - Benzenesulfonyl group - Benzoic acid or derivatives - Benzoyl - Chlorobenzene - N-alkylpiperazine - N-methylpiperazine - Halobenzene - Aryl chloride - Aryl halide - 1,4-diazinane - Piperazine - Organosulfonic acid amide - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary aliphatic amine - Amino acid or derivatives - Tertiary amine - Carboxylic acid hydrazide - Azacycle - Carboxylic acid derivative - Organoheterocyclic compound - Organic nitrogen compound - Amine - Hydrochloride - Organohalogen compound - Organochloride - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen 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