Compound Identification
SMILES
CN(C)N.CC1=CC(=O)C(C(O)(C(F)(F)Cl)C(F)(F)Cl)C(C)(C)C1
InChIKey
InChIKey=AADFFLOGACNXJB-UHFFFAOYSA-N
Formula
C14H22Cl2F4N2O2
Mass
397.24
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 Tertiary alcohols Fluorohydrins Chlorohydrins Organofluorides Organochlorides Organic oxides Hydrocarbon derivatives Alkyl fluorides Alkyl chlorides
Molecular Framework
Not available
Substituents
P-menthane monoterpenoid - Monocyclic monoterpenoid - Cyclohexenone - Tertiary alcohol - Chlorohydrin - Fluorohydrin - Halohydrin - Cyclic ketone - Ketone - Alcohol - Organochloride - Organohalogen compound - Organofluoride - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - Alkyl chloride - 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