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

InChIKey=DRCFLXIOEWYWOG-UHFFFAOYSA-N

C34H36Br2Cl2N2O4S3

863.56

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Sulfanilides Benzenesulfonyl compounds Sulfur mustard compounds Bromobenzenes Aryl bromides Organosulfonamides Aminosulfonyl compounds Dialkylthioethers Sulfenyl compounds Organic oxides Hydrocarbon derivatives Organonitrogen compounds Alkyl chlorides Organobromides Organochlorides

Aromatic homomonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Bromobenzene - Halobenzene - Sulfur mustard - Aryl bromide - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Aminosulfonyl compound - Sulfonyl - Sulfenyl compound - Dialkylthioether - Thioether - Alkyl chloride - Organosulfur compound - Organonitrogen compound - Organochloride - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Alkyl halide - Organic nitrogen 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