CC(C)(CC(N)(CC1=CC(Cl)=CC(=C1)C#N)C(F)(F)F)C1=C(O)C=CC(F)=C1

InChIKey=XSIHWNAGTPNZOE-UHFFFAOYSA-N

C20H19ClF4N2O

414.83

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Amphetamines and derivatives Phenylpropanes P-fluorophenols Benzonitriles 1-hydroxy-2-unsubstituted benzenoids Aralkylamines Chlorobenzenes Fluorobenzenes Aryl chlorides Aryl fluorides Nitriles Alkyl fluorides Organooxygen compounds Organochlorides Organofluorides Monoalkylamines Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Norlignan skeleton - Amphetamine or derivatives - Phenylpropane - Benzonitrile - 4-halophenol - 4-fluorophenol - 1-hydroxy-2-unsubstituted benzenoid - Chlorobenzene - Fluorobenzene - Aralkylamine - Halobenzene - Phenol - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Benzenoid - Carbonitrile - Nitrile - Organonitrogen compound - Organooxygen compound - Primary amine - Hydrocarbon derivative - Cyanide - Organic oxygen compound - Organic nitrogen compound - Amine - Alkyl halide - Alkyl fluoride - Primary aliphatic amine - Organohalogen compound - Organochloride - Organofluoride - Aromatic homomonocyclic 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