CN(CCC1CCN(C)CC1)C(=O)CCC1=C(C=CC(F)=C1F)N(C)S(=O)(=O)C1=C(C)C=C(Cl)C(C)=C1

InChIKey=CEIPZEVLPMIZQS-UHFFFAOYSA-N

C27H36ClF2N3O3S

556.11

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds p-Xylenes Fluorobenzenes Chlorobenzenes Piperidines Organosulfonamides Aryl chlorides Aryl fluorides Tertiary carboxylic acid amides Aminosulfonyl compounds Trialkylamines Amino acids and derivatives Azacyclic compounds Organofluorides Hydrocarbon derivatives Organic oxides Organochlorides Carbonyl compounds

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - P-xylene - Xylene - Chlorobenzene - Fluorobenzene - Halobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Piperidine - Organosulfonic acid amide - Aminosulfonyl compound - Tertiary carboxylic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary aliphatic amine - Tertiary amine - Amino acid or derivatives - Carboxamide group - Carboxylic acid derivative - Azacycle - Organoheterocyclic compound - Organic oxygen compound - Amine - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organic nitrogen 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