Compound Identification
SMILES
CC1=CC(=NN2CCOCC2)C(C(O)(C(F)(F)F)C(F)(F)F)C(C)(C)C1
InChIKey
InChIKey=MTTBFVUQPVUQHG-UHFFFAOYSA-N
Formula
C16H22F6N2O2
Mass
388.354
Taxonomic Classification
Taxonomy Tree
-
Kingdom
Organic compounds
-
Superclass
Lipids and lipid-like molecules
-
Class
Prenol lipids
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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 Morpholines Tertiary alcohols N-alkylated hydrazones Fluorohydrins Oxacyclic compounds Dialkyl ethers Azacyclic compounds Organofluorides Hydrocarbon derivatives Alkyl fluorides
Molecular Framework
Aliphatic heteromonocyclic compounds
Substituents
Monocyclic monoterpenoid - P-menthane monoterpenoid - Morpholine - Oxazinane - Tertiary alcohol - Fluorohydrin - Halohydrin - N-alkylated hydrazone - Organoheterocyclic compound - Azacycle - Dialkyl ether - Ether - Hydrazone - Oxacycle - Organic oxygen compound - Organic nitrogen compound - Alkyl fluoride - Alcohol - Organohalogen compound - Organofluoride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Alkyl halide - 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