Compound Identification
SMILES
CCCC(O)(C(C)=O)C(=S)OCCOC1CC(C)CCC1C(C)C
InChIKey
InChIKey=CWXIKFGCUPBPIK-UHFFFAOYSA-N
Formula
C19H34O4S
Mass
358.54
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
-
Subclass
Monoterpenoids
- Level 5 Menthane monoterpenoids
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Subclass
Monoterpenoids
-
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
Menthane monoterpenoids
Alternative Parents
Monocyclic monoterpenoids Acyloins Tertiary alcohols Alpha-hydroxy ketones Thioesters Carbothioic O-esters Dialkyl ethers Thiocarbonyl compounds Organic oxides Hydrocarbon derivatives
Molecular Framework
Aliphatic homomonocyclic compounds
Substituents
P-menthane monoterpenoid - Monocyclic monoterpenoid - Acyloin - Alpha-hydroxy ketone - Tertiary alcohol - Ketone - Carbothioic o-ester - Thiocarboxylic acid ester - Dialkyl ether - Ether - Thiocarboxylic acid or derivatives - Hydrocarbon derivative - Alcohol - Organic oxygen compound - Carbonyl group - Organic oxide - Organooxygen compound - Organosulfur compound - Thiocarbonyl group - Aliphatic homomonocyclic compound
Description
This compound belongs to the class of organic compounds known as menthane monoterpenoids. These are monoterpenoids with a structure based on the o-, m-, or p-menthane backbone. P-menthane consists of the cyclohexane ring with a methyl group and a (2-methyl)-propyl group at the 1 and 4 ring position, respectively. The o- and m- menthanes are much rarer, and presumably arise by alkyl migration of p-menthanes.
External Descriptors
Not available