COC(=O)C1=CC(=CC=C1)C(CC(=O)C1=CC=C(F)C=C1)CC(=O)C1=CC=C(F)C=C1

InChIKey=DEJSQEFPOZWGSD-UHFFFAOYSA-N

C25H20F2O4

422.428

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Retro-dihydrochalcones Alkyl-phenylketones Butyrophenones Benzoic acid esters Benzoyl derivatives Aryl alkyl ketones Fluorobenzenes Aryl fluorides Methyl esters Organofluorides Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Norlignan skeleton - Retro-dihydrochalcone - Linear 1,3-diarylpropanoid - Alkyl-phenylketone - Butyrophenone - Benzoate ester - Benzoic acid or derivatives - Phenylketone - Benzoyl - Aryl alkyl ketone - Aryl ketone - Halobenzene - Fluorobenzene - Benzenoid - Aryl halide - Aryl fluoride - Monocyclic benzene moiety - Methyl ester - Ketone - Carboxylic acid ester - Carboxylic acid derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Organohalogen compound - Organofluoride - Hydrocarbon derivative - 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