CC(C)N(CC1=C(F)C=CC(F)=C1)C(=O)NC1=CC=C(C=C1)S(=O)(=O)N1CCC(CNC[C@H](O)C2=CC(NS(C)(=O)=O)=C(O)C=C2)CC1

InChIKey=LSHLFPZRBGUDCA-HKBQPEDESA-N

C32H41F2N5O7S2

709.82

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides N-phenylureas Benzenesulfonyl compounds 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Fluorobenzenes Aryl fluorides Piperidines Organosulfonamides Organic sulfonamides Aminosulfonyl compounds Ureas Secondary alcohols 1,2-aminoalcohols Tertiary amines Dialkylamines Azacyclic compounds Carbonyl compounds Aromatic alcohols Hydrocarbon derivatives Organofluorides Organic oxides

Aromatic heteromonocyclic compounds

Benzenesulfonamide - N-phenylurea - Sulfanilide - Benzenesulfonyl group - 1-hydroxy-2-unsubstituted benzenoid - Fluorobenzene - Halobenzene - Aralkylamine - Phenol - Aryl fluoride - Aryl halide - Piperidine - Organic sulfonic acid amide - Organosulfonic acid amide - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Urea - Secondary alcohol - Tertiary amine - 1,2-aminoalcohol - Secondary amine - Secondary aliphatic amine - Azacycle - Organoheterocyclic compound - Amine - Organofluoride - Organohalogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organosulfur compound - Carbonyl group - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Alcohol - Aromatic alcohol - 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