1.02011-09-26 22:55:20 UTC2015-07-21 07:00:41 UTCFDB029728(E)-p-mentha-6,8-dien-2-hydroperoxideFlavouring compound [Flavornet]C10H16O2168.236168.1150297552-methyl-5-(prop-1-en-2-yl)cyclohex-1-ene-1-peroxol2-methyl-5-(prop-1-en-2-yl)cyclohex-1-ene-1-peroxol94268-57-2CC(=C)C1CCC(C)=C(C1)OOInChI=1S/C10H16O2/c1-7(2)9-5-4-8(3)10(6-9)12-11/h9,11H,1,4-6H2,2-3H3DFRLEMOBFUQIEQ-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 monoterpenoidsOrganic compoundsLipids and lipid-like moleculesPrenol lipidsMonoterpenoidsAliphatic homomonocyclic compoundsHydrocarbon derivativesMonocyclic monoterpenoidsOrganic hydroperoxidesPeroxolsAliphatic homomonocyclic compoundHydrocarbon derivativeHydroperoxideMonocyclic monoterpenoidOrganic oxygen compoundOrganooxygen compoundP-menthane monoterpenoidPeroxollogp2.97logs-1.88solubility2.21e+00 g/llogp2.31pka_strongest_acidic11.52pka_strongest_basic-4.3iupac2-methyl-5-(prop-1-en-2-yl)cyclohex-1-ene-1-peroxolaverage_mass168.236mono_mass168.115029755smilesCC(=C)C1CCC(C)=C(C1)OOformulaC10H16O2inchiInChI=1S/C10H16O2/c1-7(2)9-5-4-8(3)10(6-9)12-11/h9,11H,1,4-6H2,2-3H3inchikeyDFRLEMOBFUQIEQ-UHFFFAOYSA-Npolar_surface_area29.46refractivity49.88polarizability18.78rotatable_bond_count2acceptor_count2donor_count1physiological_charge0formal_charge0Specdb::MsMs1257667Specdb::MsMs1257668Specdb::MsMs1257669Specdb::MsMs1372825Specdb::MsMs1372826Specdb::MsMs1372827Specdb::MsMs3607300Specdb::MsMs3607301Specdb::MsMs3607302Specdb::MsMs3608311Specdb::MsMs3608312Specdb::MsMs3608313turpentine