CN(C)C1=CC=C(C=C1)C(C[Si](C)(C)C)(C(CC(=O)C1=CC=CC=C1)C1=CC=CC=C1)N1N=NC2=CC=CC=C12

InChIKey=DPMHEDHPSSJXJW-UHFFFAOYSA-N

C34H38N4OSi

546.79

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

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Lignans, neolignans and related compounds

Retro-dihydrochalcones Stilbenes Alkyl-phenylketones Phenylbutylamines Butyrophenones Benzotriazoles Aniline and substituted anilines Aryl alkyl ketones Dialkylarylamines Benzoyl derivatives Triazoles Heteroaromatic compounds Organic metalloid salts Azacyclic compounds Organic oxides Hydrocarbon derivatives Alkylsilanes

Aromatic heteropolycyclic compounds

Norlignan skeleton - Retro-dihydrochalcone - Linear 1,3-diarylpropanoid - Stilbene - Alkyl-phenylketone - Phenylbutylamine - Butyrophenone - Benzotriazole - Phenylketone - Benzoyl - Aryl ketone - Aniline or substituted anilines - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Aryl alkyl ketone - Benzenoid - Monocyclic benzene moiety - Azole - Heteroaromatic compound - Triazole - 1,2,3-triazole - Tertiary amine - Ketone - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Amine - Organonitrogen compound - Organic metalloid moeity - Organooxygen compound - Alkylsilane - Organosilicon compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic 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