Compound Identification
SMILES
CC(=C)[C@@H]1CC[C@](C)(O)[C@H](C1)[N+]1(O)CCOCC1
InChIKey
InChIKey=MRJQEOAAKUHYRC-RDBSUJKOSA-N
Formula
C14H26NO3
Mass
256.365
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
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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
Menthane monoterpenoids
Alternative Parents
Monocyclic monoterpenoids Cyclohexanols Morpholines Tertiary alcohols Cyclic alcohols and derivatives Oxacyclic compounds N-organohydroxylamines Dialkyl ethers Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives Organic cations
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Monocyclic monoterpenoid - P-menthane monoterpenoid - Cyclohexanol - Morpholine - Oxazinane - Cyclic alcohol - Tertiary alcohol - Dialkyl ether - Ether - Oxacycle - Azacycle - N-organohydroxylamine - Organoheterocyclic compound - Organonitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Organooxygen compound - Organic nitrogen compound - Organic oxygen compound - Alcohol - Organic cation - 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