1.0 2010-04-08 22:12:10 UTC 2019-11-26 03:12:34 UTC FDB015991 p-Mentha-1,3,8-triene Isolated from Petroselinum sativum (Yugoslavian parsley). p-Mentha-1,3,8-triene is found in dill, herbs and spices, and parsley. 1-Isopropenyl-4-methyl-1,3-cyclohexadiene 1-Methyl-4-(1-methylethenyl)-1,3-cyclohexadiene, 9CI 1,3-Cyclohexadiene, 2-methyl-5-(1-methylethenyl)- 1,3,8-menthatriene 1,3,8-p-menthatriene 1,3,8-para-Menthatriene 2-Methyl-5-(1-methylethenyl)-1,3-cyclohexadiene p-1,3,8-Menthatriene p-Menta-1,3,8-triene C10H14 134.2182 134.109550448 1-methyl-4-(prop-1-en-2-yl)cyclohexa-1,3-diene 1-methyl-4-(prop-1-en-2-yl)cyclohexa-1,3-diene 18368-95-1 CC(=C)C1=CC=C(C)CC1 InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4,6H,1,5,7H2,2-3H3 XNMPFDIYAMOYRM-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 Branched unsaturated hydrocarbons Cyclic olefins Monocyclic monoterpenoids Unsaturated aliphatic hydrocarbons Aliphatic homomonocyclic compound Branched unsaturated hydrocarbon Cyclic olefin Hydrocarbon Monocyclic monoterpenoid Olefin P-menthane monoterpenoid Unsaturated aliphatic hydrocarbon Unsaturated hydrocarbon logp 4.15 ALOGPS logs -2.23 ALOGPS solubility 7.94e-01 g/l ALOGPS logp 2.81 ChemAxon iupac 1-methyl-4-(prop-1-en-2-yl)cyclohexa-1,3-diene ChemAxon average_mass 134.2182 ChemAxon mono_mass 134.109550448 ChemAxon smiles CC(=C)C1=CC=C(C)CC1 ChemAxon formula C10H14 ChemAxon inchi InChI=1S/C10H14/c1-8(2)10-6-4-9(3)5-7-10/h4,6H,1,5,7H2,2-3H3 ChemAxon inchikey XNMPFDIYAMOYRM-UHFFFAOYSA-N ChemAxon polar_surface_area 0 ChemAxon refractivity 47.33 ChemAxon polarizability 16.98 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 0 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 20376 Specdb::CMs 152173 Specdb::MsMs 98508 Specdb::MsMs 98509 Specdb::MsMs 98510 Specdb::MsMs 163446 Specdb::MsMs 163447 Specdb::MsMs 163448 Specdb::MsMs 2733989 Specdb::MsMs 2733990 Specdb::MsMs 2733991 Specdb::MsMs 2971938 Specdb::MsMs 2971939 Specdb::MsMs 2971940 HMDB37013 #<Reference:0x000055ce31c0d0c8> Celery stalks Type 1 specific Apium graveolens var. dulce 117781 Dill Type 1 specific Anethum graveolens 40922 Herbs and Spices Unknown generic Parsley Type 1 specific Petroselinum crispum 4043 5.934 8.7 3.168 mg/100 g camphor herbal turpentine woody