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

InChIKey=YDVCNZCICVKGBT-UHFFFAOYSA-N

C29H27Cl2N3O5S2

632.57

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 m-Xylenes N-arylamides Dichlorobenzenes Organosulfonamides Aryl chlorides Aminosulfonyl compounds Secondary carboxylic acid amides Organic oxides Organochlorides Carbonyl compounds Hydrocarbon derivatives

Aromatic homomonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Anilide - 1,4-dichlorobenzene - M-xylene - Xylene - N-arylamide - Chlorobenzene - Halobenzene - Organosulfonic acid amide - Aryl chloride - Aryl halide - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organohalogen compound - Organochloride - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Organosulfur 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