CC1=CC=C(C=C1)S(=O)(=O)N(CC(=O)N\N=C/C1=CC=C(OCC2=CC=C(Cl)C=C2)C=C1)C1=CC=CC=C1F

InChIKey=SYHGBRRCQCNHBL-CAQPMQTCSA-N

C29H25ClFN3O4S

566.04

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Sulfanilides Alpha amino acids and derivatives Benzenesulfonamides Benzenesulfonyl compounds Phenoxy compounds Phenol ethers Alkyl aryl ethers Chlorobenzenes Fluorobenzenes Organosulfonamides Aryl chlorides Aryl fluorides Aminosulfonyl compounds Organochlorides Organofluorides Organonitrogen compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Phenoxy compound - Phenol ether - Alkyl aryl ether - Halobenzene - Fluorobenzene - Chlorobenzene - Aryl chloride - Aryl fluoride - Aryl halide - Organosulfonic acid amide - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Carboxylic acid derivative - Ether - Organofluoride - Organic oxygen compound - Organonitrogen compound - Organic nitrogen compound - Carbonyl group - Organooxygen compound - Organosulfur compound - Hydrocarbon derivative - Organic oxide - Organochloride - Organohalogen compound - Aromatic homomonocyclic compound

This compound belongs to the class of organic compounds known as n,n-disubstituted p-toluenesulfonamides. These are p-toluenesulfonamide derivatives in which the sulfonamide moiety is N,N-disubstituted.

Not available