CC1=CC=C(C=C1)S(=O)(=O)N(CC(=O)NC1=CC=C(C=C1)C1=NC2=C(S1)C=C(C)C=C2)C1=CC=C(Br)C=C1

InChIKey=FHLCZWARXMJUMH-UHFFFAOYSA-N

C29H24BrN3O3S2

606.55

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 Benzothiazoles Benzenesulfonyl compounds N-arylamides Bromobenzenes Organosulfonamides Aryl bromides Thiazoles Aminosulfonyl compounds Heteroaromatic compounds Secondary carboxylic acid amides Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organobromides

Aromatic heteropolycyclic compounds

N,n-disubstituted p-toluenesulfonamide - Alpha-amino acid or derivatives - Benzenesulfonamide - Sulfanilide - 1,3-benzothiazole - Anilide - Benzenesulfonyl group - N-arylamide - Bromobenzene - Halobenzene - Aryl bromide - Aryl halide - Organosulfonic acid amide - Sulfonyl - Heteroaromatic compound - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Aminosulfonyl compound - Thiazole - Azole - Secondary carboxylic acid amide - Carboxamide group - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Organic oxide - Organohalogen compound - Carbonyl group - Organobromide - Organic nitrogen compound - Organic oxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organosulfur compound - Aromatic heteropolycyclic 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