1.0 2010-04-08 22:06:02 UTC 2019-11-26 02:59:43 UTC FDB003972 p-Mentha-trans-1(7)-8-dien-2-ol (2s,4r)-p-mentha-1(7),8-dien-2-ol 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 (2s,4r)-p-mentha-1(7),8-dien-2-ol is slightly soluble (in water) and an extremely weak acidic compound (based on its pKa). (2s,4r)-p-mentha-1(7),8-dien-2-ol can be found in herbs and spices, which makes (2s,4r)-p-mentha-1(7),8-dien-2-ol a potential biomarker for the consumption of this food product. C10H16O 152.2334 152.120115134 (1S,5R)-2-methylidene-5-(prop-1-en-2-yl)cyclohexan-1-ol (1S,5R)-2-methylidene-5-(prop-1-en-2-yl)cyclohexan-1-ol CC(=C)C1CCC(=C)C(O)C1 InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h9-11H,1,3-6H2,2H3 PNVTXOFNJFHXOK-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 Cyclic alcohols and derivatives Hydrocarbon derivatives Monocyclic monoterpenoids Secondary alcohols Alcohol Aliphatic homomonocyclic compound Cyclic alcohol Hydrocarbon derivative Monocyclic monoterpenoid Organic oxygen compound Organooxygen compound P-menthane monoterpenoid Secondary alcohol logp 2.05 ChemAxon pka_strongest_acidic 18.21 ChemAxon pka_strongest_basic -1.4 ChemAxon iupac (1S,5R)-2-methylidene-5-(prop-1-en-2-yl)cyclohexan-1-ol ChemAxon average_mass 152.2334 ChemAxon mono_mass 152.120115134 ChemAxon smiles CC(=C)C1CCC(=C)C(O)C1 ChemAxon formula C10H16O ChemAxon inchi InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h9-11H,1,3-6H2,2H3 ChemAxon inchikey PNVTXOFNJFHXOK-UHFFFAOYSA-N ChemAxon polar_surface_area 20.23 ChemAxon refractivity 46.92 ChemAxon polarizability 17.96 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 1 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Spearmint Type 1 specific Mentha spicata 29719 Wild celery Type 1 specific Apium graveolens 4045