OC(=O)C(F)(F)F.OC(=O)C(F)(F)F.COC(=O)CC(CCC1=CC=C(C=C1)C(N)=N)C1=CC=CC(=C1)C(N)=N

InChIKey=DLMVRJSAVKRERR-UHFFFAOYSA-N

C24H26F6N4O6

580.484

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Fatty acid methyl esters Benzene and substituted derivatives Methyl esters Alpha-halocarboxylic acids Monocarboxylic acids and derivatives Carboxylic acids Carboximidamides Carboxamidines Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides

Not available

Norlignan skeleton - Linear 1,3-diarylpropanoid - Fatty acid methyl ester - Fatty acid ester - Monocyclic benzene moiety - Fatty acyl - Benzenoid - Alpha-halocarboxylic acid - Alpha-halocarboxylic acid or derivatives - Methyl ester - Carboxylic acid ester - Amidine - Carboxylic acid amidine - Carboxylic acid derivative - Carboxylic acid - Carboximidamide - Monocarboxylic acid or derivatives - Organic oxygen compound - Hydrocarbon derivative - Organic nitrogen compound - Alkyl halide - Carbonyl group - Organic oxide - Alkyl fluoride - Organooxygen compound - Organohalogen compound - Organofluoride - Organonitrogen 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