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Structure Information
Structure

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

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Taxonomic Classification

Taxonomy Tree

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

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

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