COC1=CC=C(C=C1)S(=O)(=O)N(CC1=C(Cl)C=C(O)C=C1)C1=CC=C(OCCN2CCCC2)C=C1

InChIKey=XJZMAUXHGCTUAC-UHFFFAOYSA-N

C26H29ClN2O5S

517.04

Organic compounds

Benzenoids

Benzene and substituted derivatives

Sulfanilides

Not available

Sulfanilides

Benzenesulfonamides Benzenesulfonyl compounds Phenoxy compounds Methoxybenzenes M-chlorophenols Anisoles 1-hydroxy-2-unsubstituted benzenoids Alkyl aryl ethers Chlorobenzenes Organosulfonamides N-alkylpyrrolidines Aryl chlorides Aminosulfonyl compounds Trialkylamines Azacyclic compounds Hydrocarbon derivatives Organic oxides Organochlorides

Aromatic heteromonocyclic compounds

Benzenesulfonamide - Sulfanilide - Benzenesulfonyl group - Phenoxy compound - Anisole - Methoxybenzene - 3-halophenol - 3-chlorophenol - Phenol ether - Alkyl aryl ether - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Halobenzene - Phenol - Aryl chloride - Aryl halide - N-alkylpyrrolidine - Organosulfonic acid amide - Pyrrolidine - Aminosulfonyl compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Tertiary amine - Tertiary aliphatic amine - Ether - Azacycle - Organoheterocyclic compound - Organosulfur compound - Organic oxygen compound - Organohalogen compound - Organochloride - Hydrocarbon derivative - Organic oxide - Amine - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as sulfanilides. These are organic aromatic compounds containing a sulfanilide moiety, with the general structure RS(=O)(=O)NC1=CC=CC=C1.

Not available