Compound Identification
SMILES
COC1=CC(=CC(OC)=C1OC)C(=O)C(=C\C1=CC(O[Si](C)(C)C(C)(C)C)=C(OC)C=C1)\C1=CC=CC=C1O
InChIKey
InChIKey=VFTFYMVWXUWAJY-XQNSMLJCSA-N
Formula
C31H38O7Si
Mass
550.723
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
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Superclass
Phenylpropanoids and polyketides
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Class
Linear 1,3-diarylpropanoids
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Subclass
Chalcones and dihydrochalcones
- Level 5 Retrochalcones
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Subclass
Chalcones and dihydrochalcones
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Class
Linear 1,3-diarylpropanoids
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Superclass
Phenylpropanoids and polyketides
Kingdom
Organic compounds
Superclass
Phenylpropanoids and polyketides
Class
Linear 1,3-diarylpropanoids
Subclass
Chalcones and dihydrochalcones
Intermediate Tree Nodes
Not available
Direct Parent
Retrochalcones
Alternative Parents
Stilbenes Cinnamic acids and derivatives Styrenes Phenoxy compounds Methoxybenzenes Anisoles Benzoyl derivatives Aryl ketones 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Alkyl aryl ethers Alpha-branched alpha,beta-unsaturated ketones Trialkylheterosilanes Acryloyl compounds Enones Organic metalloid salts Hydrocarbon derivatives Organic oxides
Molecular Framework
Aromatic homomonocyclic compounds
Substituents
Retrochalcone - Stilbene - Cinnamic acid or derivatives - Phenoxy compound - Benzoyl - Phenol ether - Styrene - Anisole - Methoxybenzene - Aryl ketone - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - Monocyclic benzene moiety - Benzenoid - Alpha-branched alpha,beta-unsaturated-ketone - Enone - Trialkylheterosilane - Acryloyl-group - Alpha,beta-unsaturated ketone - Ketone - Organoheterosilane - Ether - Organic metalloid salt - Organic oxygen compound - Organic metalloid moeity - Organooxygen compound - Organosilicon compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as retrochalcones. These are a form of normal chalcones that are structurally distinguished by the lack of oxygen functionalities at the C2'- and C6'-positions.
External Descriptors
Not available