OC(=O)C(CC1=CC=CC=C1)C(F)(F)C(=O)C1=CC2=C(OC3=CC=CC=C23)C=C1

InChIKey=VWRNESAOSANXFV-UHFFFAOYSA-N

C23H16F2O4

394.374

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Dibenzofurans Phenylpropanoic acids Butyrophenones Aryl alkyl ketones Gamma-keto acids and derivatives Halogenated fatty acids Alpha-haloketones Furans Heteroaromatic compounds Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organic oxides Alkyl fluorides Organofluorides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Norlignan skeleton - Dibenzofuran - 3-phenylpropanoic-acid - Butyrophenone - Benzofuran - Gamma-keto acid - Aryl ketone - Aryl alkyl ketone - Halogenated fatty acid - Keto acid - Benzenoid - Monocyclic benzene moiety - Fatty acyl - Alpha-haloketone - Furan - Heteroaromatic compound - Ketone - Carboxylic acid derivative - Carboxylic acid - Oxacycle - Organoheterocyclic compound - Monocarboxylic acid or derivatives - Alkyl halide - Alkyl fluoride - Carbonyl group - Hydrocarbon derivative - Organic oxygen compound - Organooxygen compound - Organofluoride - Organohalogen compound - Organic oxide - Aromatic heteropolycyclic 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