COC1=C(OC)C=C(C=C1)C(=O)CC(C(C#N)C#N)C1=CC2=CC=CC=C2C=C1

InChIKey=OXZUMKDAUQVOIT-UHFFFAOYSA-N

C24H20N2O3

384.435

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Retro-dihydrochalcones Alkyl-phenylketones Butyrophenones Naphthalenes Dimethoxybenzenes Phenoxy compounds Benzoyl derivatives Aryl alkyl ketones Anisoles Alkyl aryl ethers Nitriles Organopnictogen compounds Organic oxides Hydrocarbon derivatives

Aromatic homopolycyclic compounds

Norlignan skeleton - Retro-dihydrochalcone - Alkyl-phenylketone - Butyrophenone - Naphthalene - Dimethoxybenzene - O-dimethoxybenzene - Phenylketone - Phenoxy compound - Phenol ether - Anisole - Methoxybenzene - Benzoyl - Aryl alkyl ketone - Aryl ketone - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Ketone - Carbonitrile - Ether - Nitrile - Organonitrogen compound - Organooxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen 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