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cis-p-Menth-2-enol

PubChem CID: 13447111

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Compound Synonyms 2-p-menthenol, cis-p-Menth-2-enol, SCHEMBL15018584
Topological Polar Surface Area 20.2
Hydrogen Bond Donor Count 1.0
Inchi Key CCJSKHHLZKFPGH-UHFFFAOYSA-N
Rotatable Bond Count 1.0
Heavy Atom Count 11.0
Compound Name cis-p-Menth-2-enol
Kingdom Organic compounds
Description Cis-p-menth-2-enol is a member of the class of compounds known as menthane monoterpenoids. Menthane monoterpenoids 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. Cis-p-menth-2-enol is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Cis-p-menth-2-enol can be found in sweet marjoram, which makes cis-p-menth-2-enol a potential biomarker for the consumption of this food product.
Exact Mass 154.136
Formal Charge 0.0
Monoisotopic Mass 154.136
Isotope Atom Count 0.0
Molecular Complexity 158.0
Hydrogen Bond Acceptor Count 1.0
Molecular Weight 154.25
Database Name fooddb_chem_all;hmdb_chem_all;pubchem
Covalent Unit Count 1.0
Defined Atom Stereocenter Count 0.0
Iupac Name 3-methyl-6-propan-2-ylcyclohexen-1-ol
Total Atom Stereocenter Count 2.0
Molecular Framework Aliphatic homomonocyclic compounds
Total Bond Stereocenter Count 0.0
Class Prenol lipids
Inchi InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h6-9,11H,4-5H2,1-3H3
Smiles CC1CCC(C(=C1)O)C(C)C
Xlogp 3.1
Superclass Lipids and lipid-like molecules
Defined Bond Stereocenter Count 0.0
Subclass Monoterpenoids
Taxonomy Direct Parent Menthane monoterpenoids
Molecular Formula C10H18O

  • 1. Outgoing r'ship FOUND_IN to/from Origanum Majorana (Plant) Rel Props:Source_db:fooddb_chem_all