[I-].[I-].CCCCC(O)(C(CC1=CC=CC=C1)C[N+]1(C)CC[N+](C)(C)CC1)C1=CC=CC=C1

InChIKey=FGGYMSPQXGWAOI-UHFFFAOYSA-L

C27H42I2N2O

664.455

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids N-methylpiperazines Aralkylamines Benzene and substituted derivatives Tetraalkylammonium salts Tertiary alcohols 1,3-aminoalcohols Azacyclic compounds Organic zwitterions Organic iodide salts Hydrocarbon derivatives Aromatic alcohols

Aromatic heteromonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - N-methylpiperazine - N-alkylpiperazine - Aralkylamine - Monocyclic benzene moiety - 1,4-diazinane - Piperazine - Benzenoid - Tetraalkylammonium salt - Quaternary ammonium salt - Tertiary alcohol - 1,3-aminoalcohol - Azacycle - Organoheterocyclic compound - Aromatic alcohol - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic nitrogen compound - Amine - Organic iodide salt - Alcohol - Organic oxygen compound - Organic zwitterion - Organic salt - Aromatic heteromonocyclic 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.

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