CC(C)(C)[Si](C)(C)O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)C1=CC=C(OC2=C(OCC3=CC=CC=C3)C=CC(CCC(O)=O)=C2)C=C1

InChIKey=PIDUHPRQFVQWSC-VLZNPVHKSA-N

C37H54O7Si2

667.002

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Diphenylethers Phenylpropanoic acids Diarylethers Phenoxy compounds Phenol ethers Alkyl aryl ethers Trialkylheterosilanes Silyl ethers Organic metalloid salts Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds

Aromatic homomonocyclic compounds

Oxyneolignan skeleton - Diphenylether - Diaryl ether - 3-phenylpropanoic-acid - Phenoxy compound - Phenol ether - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Trialkylheterosilane - Silyl ether - Organoheterosilane - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organic metalloid salt - Hydrocarbon derivative - Alcohol - Organic oxide - Carbonyl group - Organic metalloid moeity - Organooxygen compound - Organic oxygen compound - Organosilicon compound - Primary alcohol - 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