CCOC1=CC=CC=C1N1CCN(CC1)S(=O)(=O)C1=CC(Cl)=C(C)C=C1

InChIKey=KDZQLWXCMFUEMF-UHFFFAOYSA-N

C19H23ClN2O3S

394.91

Organic compounds

Benzenoids

Benzene and substituted derivatives

Toluenes

Tosyl compounds - P-toluenesulfonamides

N,N-disubstituted p-toluenesulfonamides

Phenylpiperazines N-arylpiperazines Benzenesulfonamides Aminophenyl ethers Benzenesulfonyl compounds Phenoxy compounds Aniline and substituted anilines Dialkylarylamines Alkyl aryl ethers Chlorobenzenes Organosulfonamides Aryl chlorides Sulfonyls Azacyclic compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

N,n-disubstituted p-toluenesulfonamide - Phenylpiperazine - N-arylpiperazine - Benzenesulfonamide - Aminophenyl ether - Benzenesulfonyl group - Phenoxy compound - Phenol ether - Tertiary aliphatic/aromatic amine - Aniline or substituted anilines - Dialkylarylamine - Alkyl aryl ether - Chlorobenzene - Halobenzene - Organosulfonic acid amide - Piperazine - Aryl chloride - Aryl halide - 1,4-diazinane - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Tertiary amine - Organoheterocyclic compound - Azacycle - Ether - Hydrocarbon derivative - Organohalogen compound - Organochloride - Organonitrogen compound - Amine - Organic nitrogen compound - Organooxygen compound - Organosulfur compound - Organic oxygen compound - Organic oxide - 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