1.0 2010-04-08 22:07:00 UTC 2025-11-18 23:00:58 UTC FDB006130 trans-Carvyl formate Trans-carvyl formate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). Trans-carvyl formate can be found in spearmint, which makes trans-carvyl formate a potential biomarker for the consumption of this food product. C11H16O2 180.247 180.115029755 (1R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl formate (1R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl formate [H][C@@]1(CC=C(C)[C@@]([H])(C1)OC=O)C(C)=C InChI=1S/C11H16O2/c1-8(2)10-5-4-9(3)11(6-10)13-7-12/h4,7,10-11H,1,5-6H2,2-3H3/t10-,11+/m0/s1 BPBPWBGJZQBEKD-WDEREUQCSA-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 Carbonyl compounds Carboxylic acid esters Hydrocarbon derivatives Monocarboxylic acids and derivatives Monocyclic monoterpenoids Organic oxides Aliphatic homomonocyclic compound Carbonyl group Carboxylic acid derivative Carboxylic acid ester Hydrocarbon derivative Monocarboxylic acid or derivatives Monocyclic monoterpenoid Organic oxide Organic oxygen compound Organooxygen compound P-menthane monoterpenoid logp 3.29 ALOGPS logs -2.41 ALOGPS solubility 7.09e-01 g/l ALOGPS logp 2.38 ChemAxon pka_strongest_basic -6.8 ChemAxon iupac (1R,5S)-2-methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-yl formate ChemAxon average_mass 180.247 ChemAxon mono_mass 180.115029755 ChemAxon smiles [H][C@@]1(CC=C(C)[C@@]([H])(C1)OC=O)C(C)=C ChemAxon formula C11H16O2 ChemAxon inchi InChI=1S/C11H16O2/c1-8(2)10-5-4-9(3)11(6-10)13-7-12/h4,7,10-11H,1,5-6H2,2-3H3/t10-,11+/m0/s1 ChemAxon inchikey BPBPWBGJZQBEKD-WDEREUQCSA-N ChemAxon polar_surface_area 26.3 ChemAxon refractivity 52.66 ChemAxon polarizability 19.97 ChemAxon rotatable_bond_count 3 ChemAxon acceptor_count 1 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 87516 Specdb::MsMs 87517 Specdb::MsMs 87518 Specdb::MsMs 150036 Specdb::MsMs 150037 Specdb::MsMs 150038 Specdb::MsMs 3602531 Specdb::MsMs 3602532 Specdb::MsMs 3602533 Specdb::MsMs 3602534 Specdb::MsMs 3602535 Specdb::MsMs 3602536 Spearmint Type 1 specific Mentha spicata 29719