Compound Identification
SMILES
CCCCCCCC[Sn++]CCCCCCCC.[O-]C(=O)C(\CC1=CC=CC=C1)=C(\CC1=CC=CC=C1)C([O-])=O
InChIKey
InChIKey=OSDGWFNSTUCYOU-SWJSCKDZSA-L
Formula
C34H48O4Sn
Mass
639.464
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
- Superclass Lignans, neolignans and related compounds
Kingdom
Organic compounds
Superclass
Lignans, neolignans and related compounds
Class
Not available
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Lignans, neolignans and related compounds
Alternative Parents
Phenylpropanoic acids Dicarboxylic acids and derivatives Benzene and substituted derivatives Carboxylic acid salts Carboxylic acids Organotin compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic cations
Molecular Framework
Not available
Substituents
Norlignan skeleton - 3-phenylpropanoic-acid - Monocyclic benzene moiety - Benzenoid - Dicarboxylic acid or derivatives - Carboxylic acid salt - Carboxylic acid derivative - Carboxylic acid - Organic oxygen compound - Carbonyl group - Organometallic compound - Organic post-transition metal moeity - Organooxygen compound - Organotin compound - Hydrocarbon derivative - Organic oxide - Organic cation - Aromatic homomonocyclic compound
Description
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.
External Descriptors
Not available