Structure Information
Structure

Compound Identification

SMILES

CCC(O)[C@]12[C@@H](C[C@H](C)[C@H]1CC[C@H](C)C2O[Si](CC)(CC)CC)C=C(C)C

InChIKey

InChIKey=WXXIWVBAICSGFM-RFTCCRLBSA-N

Formula

C24H46O2Si

Mass

394.715

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Taxonomic Classification

Taxonomy Tree

Kingdom

Organic compounds

Superclass

Lipids and lipid-like molecules

Class

Prenol lipids

Subclass

Diterpenoids

Intermediate Tree Nodes

Not available

Direct Parent

Elisabethane diterpenoids

Alternative Parents

Molecular Framework

Aliphatic homopolycyclic compounds

Substituents

Elisabethane diterpenoid - Trialkylheterosilane - Silyl ether - Secondary alcohol - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organosilicon compound - Organooxygen compound - Organic metalloid moeity - Alcohol - Aliphatic homopolycyclic compound

Description

This compound belongs to the class of organic compounds known as elisabethane diterpenoids. These are diterpenoids with a structure based on the elisabethane skeleton, a tricyclic serrulatane derivative that is formed by connecting the C1 and C9 atom of serrulatane. This class of compounds also includes seco-elisabethane derivatives, nor-elisabethanes (resulting from the loss of one carbon atom), and bisnor-elisabethanes (resulting from the loss of two carbon atoms).

External Descriptors

Not available

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