COC1=C(OC2CCCC2)C=C(C=C1)C(CC(O)=O)C#CC1=CC=C(Cl)C=C1

InChIKey=CPIOZVZLDARBEC-UHFFFAOYSA-N

C23H23ClO4

398.88

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Phenylpropanoic acids Phenoxy compounds Anisoles Methoxybenzenes Medium-chain fatty acids Alkyl aryl ethers Chlorobenzenes Halogenated fatty acids Unsaturated fatty acids Aryl chlorides Monocarboxylic acids and derivatives Carboxylic acids Carbonyl compounds Organochlorides Organic oxides Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - 3-phenylpropanoic-acid - Phenoxy compound - Anisole - Methoxybenzene - Medium-chain fatty acid - Phenol ether - Alkyl aryl ether - Halogenated fatty acid - Halobenzene - Chlorobenzene - Unsaturated fatty acid - Aryl halide - Monocyclic benzene moiety - Benzenoid - Fatty acid - Fatty acyl - Aryl chloride - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organic oxygen compound - Carbonyl group - Organochloride - Organooxygen compound - Organic oxide - Organohalogen compound - 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