1.0 2010-04-08 22:07:06 UTC 2025-11-18 23:01:37 UTC FDB006339 cis-p-Menth-2-enol 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. C10H18O 154.2493 154.135765198 3-methyl-6-(propan-2-yl)cyclohex-1-en-1-ol 6-isopropyl-3-methylcyclohex-1-en-1-ol CC(C)C1CCC(C)C=C1O InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h6-9,11H,4-5H2,1-3H3 CCJSKHHLZKFPGH-UHFFFAOYSA-N 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. Menthane monoterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Monoterpenoids Aliphatic homomonocyclic compounds Enols Hydrocarbon derivatives Monocyclic monoterpenoids Aliphatic homomonocyclic compound Enol Hydrocarbon derivative Monocyclic monoterpenoid Organic oxygen compound Organooxygen compound P-menthane monoterpenoid logp 3.25 ALOGPS logs -2.28 ALOGPS solubility 8.09e-01 g/l ALOGPS logp 2.86 ChemAxon pka_strongest_acidic 10.63 ChemAxon pka_strongest_basic -4.7 ChemAxon iupac 3-methyl-6-(propan-2-yl)cyclohex-1-en-1-ol ChemAxon average_mass 154.2493 ChemAxon mono_mass 154.135765198 ChemAxon smiles CC(C)C1CCC(C)C=C1O ChemAxon formula C10H18O ChemAxon inchi InChI=1S/C10H18O/c1-7(2)9-5-4-8(3)6-10(9)11/h6-9,11H,4-5H2,1-3H3 ChemAxon inchikey CCJSKHHLZKFPGH-UHFFFAOYSA-N ChemAxon polar_surface_area 20.23 ChemAxon refractivity 48.94 ChemAxon polarizability 18.85 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 1 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 108864 Specdb::MsMs 108865 Specdb::MsMs 108866 Specdb::MsMs 176181 Specdb::MsMs 176182 Specdb::MsMs 176183 Specdb::MsMs 3602834 Specdb::MsMs 3602835 Specdb::MsMs 3602836 Specdb::MsMs 3604004 Specdb::MsMs 3604005 Specdb::MsMs 3604006 Sweet marjoram Type 1 specific Origanum majorana 268884