CC1=CC(CC(N)(CC(C)(C)C2=C(O)C=CC(F)=C2)C(F)(F)F)=CC(C)=C1C#N

InChIKey=FSDCKBRGTQSLDQ-UHFFFAOYSA-N

C22H24F4N2O

408.441

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

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

Aromatic homomonocyclic compounds

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