1.0 2026-09-23 00:01:22 UTC 2026-09-23 00:01:22 UTC FDB119145 (+)-2-Carene (1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene C10H16 136.238 136.125200515 (1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene (1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene CC1=C[C@H]2[C@@H](CC1)C2(C)C InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6,8-9H,4-5H2,1-3H3/t8-,9+/m1/s1 IBVJWOMJGCHRRW-BDAKNGLRSA-N belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other. Bicyclic monoterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Monoterpenoids Aliphatic homopolycyclic compounds Branched unsaturated hydrocarbons Cyclic olefins Polycyclic hydrocarbons Unsaturated aliphatic hydrocarbons Aliphatic homopolycyclic compound Bicyclic monoterpenoid Branched unsaturated hydrocarbon Carane monoterpenoid Cyclic olefin Hydrocarbon Olefin Polycyclic hydrocarbon Unsaturated aliphatic hydrocarbon Unsaturated hydrocarbon logp 3.26 ALOGPS logs -2.95 ALOGPS solubility 1.51e-01 g/l ALOGPS logp 2.8 ChemAxon iupac (1S,6R)-3,7,7-trimethylbicyclo[4.1.0]hept-2-ene ChemAxon average_mass 136.238 ChemAxon mono_mass 136.125200515 ChemAxon smiles CC1=C[C@H]2[C@@H](CC1)C2(C)C ChemAxon formula C10H16 ChemAxon inchi InChI=1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6,8-9H,4-5H2,1-3H3/t8-,9+/m1/s1 ChemAxon inchikey IBVJWOMJGCHRRW-BDAKNGLRSA-N ChemAxon polar_surface_area 0 ChemAxon refractivity 44.72 ChemAxon polarizability 17.29 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 0 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon