CC(N(C1=C(F)C=CC(F)=C1)S(=O)(=O)C1=CC=C(Cl)C=C1)C1=NC=C(CCC(=O)N2CCC(O)CC2)S1

InChIKey=URSSWURSBCVYRL-UHFFFAOYSA-N

C25H26ClF2N3O4S2

570.07

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds N-acylpiperidines 2,5-disubstituted thiazoles Chlorobenzenes Fluorobenzenes Aryl chlorides Organosulfonamides Aryl fluorides Tertiary carboxylic acid amides Aminosulfonyl compounds Heteroaromatic compounds Secondary alcohols Azacyclic compounds Carbonyl compounds Organochlorides Organofluorides Organonitrogen compounds Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - N-acyl-piperidine - 2,5-disubstituted 1,3-thiazole - Halobenzene - Fluorobenzene - Chlorobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Piperidine - Organosulfonic acid amide - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Sulfonyl - Tertiary carboxylic acid amide - Thiazole - Aminosulfonyl compound - Azole - Heteroaromatic compound - Carboxamide group - Secondary alcohol - Carboxylic acid derivative - Organoheterocyclic compound - Azacycle - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alcohol - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organochloride - Organofluoride - 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