COC1=C(C=C(F)C=C1)C(C)(C)CC(O)(CC1=C(Cl)C=C(C=C1)C#N)C(F)(F)F

InChIKey=AAJNWJFLYOFHIB-UHFFFAOYSA-N

C21H20ClF4NO2

429.84

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Phenylpropanes Phenoxy compounds Anisoles Methoxybenzenes Benzonitriles Alkyl aryl ethers Fluorobenzenes Chlorobenzenes Aryl chlorides Aryl fluorides Tertiary alcohols Fluorohydrins Nitriles Hydrocarbon derivatives Organochlorides Alkyl fluorides Organofluorides

Aromatic homomonocyclic compounds

Norlignan skeleton - Phenylpropane - Anisole - Benzonitrile - Phenol ether - Phenoxy compound - Methoxybenzene - Alkyl aryl ether - Chlorobenzene - Fluorobenzene - Halobenzene - Benzenoid - Aryl chloride - Aryl fluoride - Aryl halide - Monocyclic benzene moiety - Tertiary alcohol - Fluorohydrin - Halohydrin - Carbonitrile - Nitrile - Ether - Organic oxygen compound - Organohalogen compound - Organochloride - Organofluoride - Organonitrogen compound - Organooxygen compound - Alkyl fluoride - Alkyl halide - Alcohol - Hydrocarbon derivative - Cyanide - Organic nitrogen 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