C[Sn](C)(Br)C(=C(C(=C(Br)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1)C1=CC=CC=C1

InChIKey=SFLFCGFZSKZPPI-UHFFFAOYSA-M

C30H26Br2Sn

665.056

Organic compounds

Lignans, neolignans and related compounds

Not available

Not available

Not available

Lignans, neolignans and related compounds

Linear 1,3-diarylpropanoids Stilbenes Benzene and substituted derivatives Triorganotin halide salts Vinyl bromides Organic metal bromide salts Metal alkyl halides Dialkyltins Bromoalkenes Organobromides Organic bromide salts Hydrocarbon derivatives

Aromatic homomonocyclic compounds

Norlignan skeleton - Linear 1,3-diarylpropanoid - Stilbene - Monocyclic benzene moiety - Benzenoid - Triorganotin halide salt - Metal alkyl halide - Dialkyltin - Vinyl bromide - Vinyl halide - Organic metal bromide salt - Haloalkene - Bromoalkene - Organic metal salt - Hydrocarbon derivative - Organohalogen compound - Organotin compound - Organic tin salt - Organic post-transition metal moeity - Organobromide - Organometallic compound - Organic bromide salt - 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