CC1=CC=C(C=C1)S(=O)(=O)N1CCC2=C(NN(C2=O)C2=CC(Cl)=C(Cl)C=C2)C2=C1N=CC=C2

InChIKey=UDVBZXKQFKMVPR-UHFFFAOYSA-N

C23H18Cl2N4O3S

501.38

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Pyrazolylpyridines Phenylpyrazoles Benzenesulfonamides Benzenesulfonyl compounds Dichlorobenzenes Azepines Organosulfonamides Imidolactams Aryl chlorides Pyrazolones Heteroaromatic compounds Sulfonyls Vinylogous amides Lactams Azacyclic compounds Organooxygen compounds Organonitrogen compounds Organochlorides Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

N,n-disubstituted p-toluenesulfonamide - Phenylpyrazole - 3-pyrazolylpyridine - Benzenesulfonamide - Benzenesulfonyl group - 1,2-dichlorobenzene - Azepine - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Pyrazolinone - Pyridine - Organosulfonic acid amide - Imidolactam - Vinylogous amide - Sulfonyl - Azole - Pyrazole - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Heteroaromatic compound - Lactam - Organoheterocyclic compound - Azacycle - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organosulfur compound - Organic oxygen compound - Organic nitrogen compound - Organohalogen compound - Organochloride - 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