CC1=CC=C(C=C1)S(=O)(=O)N(CC(=O)NC1=CC=C(C=C1)S(=O)(=O)NC1=CC=C(Br)C=C1)C1=CC(Cl)=C(Cl)C=C1

InChIKey=TZFYAUGLIHKWNN-UHFFFAOYSA-N

C27H22BrCl2N3O5S2

683.41

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Sulfanilides Alpha amino acids and derivatives Benzenesulfonamides Anilides Benzenesulfonyl compounds N-arylamides Dichlorobenzenes Bromobenzenes Organosulfonamides Aryl bromides Aryl chlorides Aminosulfonyl compounds Secondary carboxylic acid amides Organobromides Organochlorides Organic oxides Carbonyl compounds Hydrocarbon derivatives

Aromatic homomonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Anilide - 1,2-dichlorobenzene - N-arylamide - Halobenzene - Chlorobenzene - Bromobenzene - Aryl bromide - Aryl chloride - Aryl halide - Organosulfonic acid amide - Sulfonyl - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Organochloride - Organonitrogen compound - Organooxygen compound - Carbonyl group - Organosulfur compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organohalogen compound - Organobromide - 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