Compound Identification
SMILES
CC#CC[C@H](C)[C@H](O[Si](C)(C)C(C)(C)C)\C=C\[C@H]1[C@@H](C[C@@H]2C\C(C[C@H]12)=C/C(=O)O[C@H]1CCCC[C@@H]1C(C)(C)C1=CC=CC=C1)O[Si](C)(C)C(C)(C)C
InChIKey
InChIKey=AIKVVUQUVULIEX-SXNIYDKZSA-N
Formula
C46H74O4Si2
Mass
747.264
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
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Subclass
Monoterpenoids
- Level 5 Bicyclic monoterpenoids
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Subclass
Monoterpenoids
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Class
Prenol lipids
-
Superclass
Lipids and lipid-like molecules
Kingdom
Organic compounds
Superclass
Lipids and lipid-like molecules
Class
Prenol lipids
Subclass
Monoterpenoids
Intermediate Tree Nodes
Not available
Direct Parent
Bicyclic monoterpenoids
Alternative Parents
Aromatic monoterpenoids Phenylpropanes Trialkylheterosilanes Enoate esters Silyl ethers Organic metalloid salts Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aromatic homopolycyclic compounds
Substituents
Aromatic monoterpenoid - Bicyclic monoterpenoid - Phenylpropane - Monocyclic benzene moiety - Benzenoid - Trialkylheterosilane - Alpha,beta-unsaturated carboxylic ester - Enoate ester - Carboxylic acid ester - Silyl ether - Organoheterosilane - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Organic metalloid salt - Hydrocarbon derivative - Organic oxygen compound - Carbonyl group - Organic metalloid moeity - Organooxygen compound - Organic oxide - Organosilicon compound - Aromatic homopolycyclic compound
Description
This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
External Descriptors
Not available