1.02010-04-08 22:06:24 UTC2019-11-26 03:00:14 UTCFDB004802trans-1-Carveol(+)-trans-carveol, also known as (1r,5s)-carveol, 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 (+)-trans-carveol is slightly soluble (in water) and an extremely weak acidic compound (based on its pKa). (+)-trans-carveol can be found in caraway and dill, which makes (+)-trans-carveol a potential biomarker for the consumption of these food products. C10H16O152.2334152.120115134(1R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol(+)-trans-carveolCC(=C)[C@H]1CC=C(C)[C@H](O)C1InChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10+/m0/s1BAVONGHXFVOKBV-VHSXEESVSA-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 monoterpenoidsOrganic compoundsLipids and lipid-like moleculesPrenol lipidsMonoterpenoidsAliphatic homomonocyclic compoundsHydrocarbon derivativesMonocyclic monoterpenoidsSecondary alcoholsAlcoholAliphatic homomonocyclic compoundHydrocarbon derivativeMonocyclic monoterpenoidOrganic oxygen compoundOrganooxygen compoundP-menthane monoterpenoidSecondary alcoholCyclic monoterpenesMenthane monoterpenoidscarveollogp2.41logs-1.73solubility2.82e+00 g/llogp1.99pka_strongest_acidic18.21pka_strongest_basic-1.4iupac(1R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-olaverage_mass152.2334mono_mass152.120115134smilesCC(=C)[C@H]1CC=C(C)[C@H](O)C1formulaC10H16OinchiInChI=1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10+/m0/s1inchikeyBAVONGHXFVOKBV-VHSXEESVSA-Npolar_surface_area20.23refractivity48polarizability18.07rotatable_bond_count1acceptor_count1donor_count1physiological_charge0formal_charge0Specdb::CMs173087Specdb::NmrOneD51422Specdb::NmrOneD51423Specdb::NmrOneD51424Specdb::NmrOneD51425Specdb::NmrOneD51426Specdb::NmrOneD51427Specdb::NmrOneD51428Specdb::NmrOneD51429Specdb::NmrOneD51430Specdb::NmrOneD51431Specdb::NmrOneD51432Specdb::NmrOneD51433Specdb::NmrOneD51434Specdb::NmrOneD51435Specdb::NmrOneD51436Specdb::NmrOneD51437Specdb::NmrOneD51438Specdb::NmrOneD51439Specdb::NmrOneD51440Specdb::NmrOneD51441Specdb::MsMs59589Specdb::MsMs59590Specdb::MsMs59591Specdb::MsMs115755Specdb::MsMs115756Specdb::MsMs115757Specdb::MsMs2725445Specdb::MsMs2725446Specdb::MsMs2725447Specdb::MsMs2956308Specdb::MsMs2956309Specdb::MsMs2956310CarawayType 1specificCarum carvi48032