Cl.NC1CCC2=C(C=C(CCCNS(=O)(=O)CC3CC3)C=C2)C1CC1=CC(Cl)=CC=C1

InChIKey=DDUKOXIBTQOILG-UHFFFAOYSA-N

C24H32Cl2N2O2S

483.49

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Tetralins Chlorobenzenes Aralkylamines Organosulfonamides Organic sulfonamides Aryl chlorides Aminosulfonyl compounds Organochlorides Organic oxides Monoalkylamines Hydrochlorides Hydrocarbon derivatives

Aromatic homopolycyclic compounds

Neolignan skeleton - Tetralin - Chlorobenzene - Halobenzene - Aralkylamine - Aryl chloride - Aryl halide - Monocyclic benzene moiety - Organic sulfonic acid amide - Organosulfonic acid amide - Benzenoid - Organosulfonic acid or derivatives - Aminosulfonyl compound - Organic sulfonic acid or derivatives - Sulfonyl - Hydrochloride - Organosulfur compound - Organonitrogen compound - Organochloride - Organohalogen compound - Primary aliphatic amine - Organic oxide - Organic oxygen compound - Amine - Primary amine - Hydrocarbon derivative - Organic nitrogen compound - Aromatic homopolycyclic compound

This compound belongs to the class of organic compounds known as lignans, neolignans and related compounds. These are plant products of low molecular weight formed primarily from oxidative coupling of two p-propylphenol moieties. They can also be described as micromolecules with two phenylpropanoid units coupled together. They can be attached in various manners, like C5-C5', C8-C8'. Most known natural lignans are oxidized at C9 and C9´ and, based upon the way in which oxygen is incorporated into the skeleton and on the cyclization patterns, a wide range of lignans of very different structural types can be formed.

Not available