Compound Identification
SMILES
CC(=C)C1CCC(C)=CC1.CC(=C)C1CC=C(C)C(=O)C1.OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O
InChIKey
InChIKey=YBDWEHBHEOKOOQ-SCRCCMNGSA-N
Formula
C26H42O7
Mass
466.615
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 Cyclohexenones Branched unsaturated hydrocarbons Polyols Cycloalkenes Unsaturated aliphatic hydrocarbons Organic oxides Hydrocarbon derivatives
Molecular Framework
Not available
Substituents
P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexenone - Branched unsaturated hydrocarbon - Cyclic ketone - Ketone - Polyol - Cycloalkene - Cyclic olefin - Organic oxygen compound - Unsaturated aliphatic hydrocarbon - Unsaturated hydrocarbon - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Olefin - Carbonyl group - Hydrocarbon - Aliphatic heteromonocyclic 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