Compound Identification
SMILES
COC1=CC(=CC(OC)=C1O)C1OC2=C(OC1CO[Si](C)(C)C(C)(C)C)C=CC(\C=C\C1=CC(O)=CC(O)=C1)=C2
InChIKey
InChIKey=CTPAHDMMTXFZCL-CMDGGOBGSA-N
Formula
C31H38O8Si
Mass
566.722
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lignans, neolignans and related compounds
- Class Stilbenolignans
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Superclass
Lignans, neolignans and related compounds
Kingdom
Organic compounds
Superclass
Lignans, neolignans and related compounds
Class
Stilbenolignans
Subclass
Not available
Intermediate Tree Nodes
Not available
Direct Parent
Stilbenolignans
Alternative Parents
Phenylbenzo-1,4-dioxanes Stilbenes Benzo-1,4-dioxanes Dimethoxybenzenes Methoxyphenols Anisoles Styrenes Phenoxy compounds Resorcinols 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers 1-hydroxy-2-unsubstituted benzenoids Para dioxins Trialkylheterosilanes Silyl ethers Organic metalloid salts Oxacyclic compounds Hydrocarbon derivatives
Molecular Framework
Aromatic heteropolycyclic compounds
Substituents
Stilbenolignan skeleton - 2-phenylbenzo-1,4-dioxane - Phenylbenzodioxane - Stilbene - Benzo-1,4-dioxane - Benzodioxane - Methoxyphenol - Dimethoxybenzene - M-dimethoxybenzene - Anisole - Phenoxy compound - Phenol ether - Resorcinol - Styrene - Methoxybenzene - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Alkyl aryl ether - Phenol - Benzenoid - Para-dioxin - Monocyclic benzene moiety - Trialkylheterosilane - Silyl ether - Organoheterosilane - Oxacycle - Ether - Organoheterocyclic compound - Organic metalloid salt - Organooxygen compound - Organic metalloid moeity - Organosilicon compound - Hydrocarbon derivative - Organic oxygen compound - Aromatic heteropolycyclic compound
Description
This compound belongs to the class of organic compounds known as stilbenolignans. These are non-conventional lignans that derived from stilbene. They are characterized by a p-dioxin ring substituted at one carbon atom by a C3C6 (phenylpropan) group and fused to one ring of the stilbene moiety.
External Descriptors
Not available