1.0 2010-04-08 22:11:33 UTC 2019-11-26 03:10:57 UTC FDB014924 (R)-p-Mentha-1,8-dien-7-ol Isolated from caraway seed oil. (R)-p-Mentha-1,8-dien-7-ol is found in herbs and spices. (+)-Perillyl alcohol (R)-(+)-Perillyl alcohol (R)-4-(1-Methylethenyl)-1-cyclohexene-1-methanol (R)-Perillyl alcohol 1-Cyclohexene-1-methanol, 4-(1-methylethenyl)-, (4R)- 4-(1-Methylethenyl)-(4R)-1-cyclohexene-1-methanol D-Perillyl alcohol C10H16O 152.2334 152.120115134 [(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol [(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol 57717-97-2 CC(=C)[C@@H]1CCC(CO)=CC1 InChI=1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,10-11H,1,4-7H2,2H3/t10-/m0/s1 NDTYTMIUWGWIMO-JTQLQIEISA-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 Hydrocarbon derivatives Monocyclic monoterpenoids Primary alcohols Alcohol Aliphatic homomonocyclic compound Hydrocarbon derivative Monocyclic monoterpenoid Organic oxygen compound Organooxygen compound P-menthane monoterpenoid Primary alcohol logp 2.50 ALOGPS logs -1.90 ALOGPS solubility 1.90e+00 g/l ALOGPS logp 1.94 ChemAxon pka_strongest_acidic 16.86 ChemAxon pka_strongest_basic -2 ChemAxon iupac [(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol ChemAxon average_mass 152.2334 ChemAxon mono_mass 152.120115134 ChemAxon smiles CC(=C)[C@@H]1CCC(CO)=CC1 ChemAxon formula C10H16O ChemAxon inchi InChI=1S/C10H16O/c1-8(2)10-5-3-9(7-11)4-6-10/h3,10-11H,1,4-7H2,2H3/t10-/m0/s1 ChemAxon inchikey NDTYTMIUWGWIMO-JTQLQIEISA-N ChemAxon polar_surface_area 20.23 ChemAxon refractivity 48.26 ChemAxon polarizability 18.18 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 1 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 12068 Specdb::CMs 44718 Specdb::CMs 132131 Specdb::CMs 136015 Specdb::CMs 139865 Specdb::CMs 143749 Specdb::MsMs 53109 Specdb::MsMs 53110 Specdb::MsMs 53111 Specdb::MsMs 134448 Specdb::MsMs 134449 Specdb::MsMs 134450 Specdb::MsMs 2664382 Specdb::MsMs 2664383 Specdb::MsMs 2664384 Specdb::MsMs 2780599 Specdb::MsMs 2780600 Specdb::MsMs 2780601 Specdb::NmrOneD 133578 Specdb::NmrOneD 133579 Specdb::NmrOneD 133580 Specdb::NmrOneD 133581 Specdb::NmrOneD 133582 Specdb::NmrOneD 133583 Specdb::NmrOneD 133584 Specdb::NmrOneD 133585 Specdb::NmrOneD 133586 Specdb::NmrOneD 133587 Specdb::NmrOneD 133588 Specdb::NmrOneD 133589 Specdb::NmrOneD 133590 Specdb::NmrOneD 133591 Specdb::NmrOneD 133592 Specdb::NmrOneD 133593 Specdb::NmrOneD 133594 Specdb::NmrOneD 133595 Specdb::NmrOneD 133596 Specdb::NmrOneD 133597 Specdb::NmrOneD 133598 Specdb::NmrOneD 133599 Specdb::NmrOneD 133600 Specdb::NmrOneD 133601 Specdb::NmrOneD 133602 HMDB36087 #<Reference:0x000055ce316efa50> Herbs and Spices Unknown generic