CC1=CC=C(C=C1)S(=O)(=O)N1CCCN(CCN(CCCN(CC2=CC(Br)=C(CN3CCCN(CCN(CCCN(CC3)S(=O)(=O)C3=CC=C(C)C=C3)S(=O)(=O)C3=CC=C(C)C=C3)S(=O)(=O)C3=CC=C(C)C=C3)C=C2)CC1)S(=O)(=O)C1=CC=C(C)C=C1)S(=O)(=O)C1=CC=C(C)C=C1

InChIKey=CPOPWKRKZVPOOV-UHFFFAOYSA-N

C70H89BrN8O12S6

1506.79

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Benzenesulfonamides Benzenesulfonyl compounds Phenylmethylamines Benzylamines Bromobenzenes Aralkylamines Organosulfonamides Aryl bromides Sulfonyls Trialkylamines Azacyclic compounds Organobromides Organic oxides Hydrocarbon derivatives

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Benzenesulfonamide - Benzenesulfonyl group - Benzylamine - Phenylmethylamine - Bromobenzene - Aralkylamine - Halobenzene - Aryl bromide - Aryl halide - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Tertiary aliphatic amine - Tertiary amine - Organoheterocyclic compound - Azacycle - Amine - Organosulfur compound - Organonitrogen compound - Organobromide - Organohalogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic heteromonocyclic 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