1.0 2026-09-21 13:28:01 UTC 2026-09-21 13:28:01 UTC FDB116506 Cannabidivarin 2-[(1R,6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]-5-propylbenzene-1,3-diol 2-[(1R,6R)-6-isopropenyl-3-methyl-cyclohex-2-en-1-yl]-5-propyl-benzene-1,3-diol C19H26O2 286.415 286.193280077 2-[(1R,6R)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-yl]-5-propylbenzene-1,3-diol 2-[(1R,6R)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-yl]-5-propylbenzene-1,3-diol [H][C@]1(CCC(C)=C[C@@]1([H])C1=C(O)C=C(CCC)C=C1O)C(C)=C InChI=1S/C19H26O2/c1-5-6-14-10-17(20)19(18(21)11-14)16-9-13(4)7-8-15(16)12(2)3/h9-11,15-16,20-21H,2,5-8H2,1,3-4H3/t15-,16+/m0/s1 REOZWEGFPHTFEI-JKSUJKDBSA-N belongs to the class of organic compounds known as aromatic monoterpenoids. These are monoterpenoids containing at least one aromatic ring. Aromatic monoterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Monoterpenoids Aromatic homomonocyclic compounds 1-hydroxy-2-unsubstituted benzenoids 1-hydroxy-4-unsubstituted benzenoids Hydrocarbon derivatives Menthane monoterpenoids Monocyclic monoterpenoids Organooxygen compounds Phenylpropanes Resorcinols 1-hydroxy-2-unsubstituted benzenoid 1-hydroxy-4-unsubstituted benzenoid Aromatic homomonocyclic compound Aromatic monoterpenoid Benzenoid Hydrocarbon derivative Monocyclic benzene moiety Monocyclic monoterpenoid Organic oxygen compound Organooxygen compound P-menthane monoterpenoid Phenol Phenylpropane Resorcinol logp 5.13 ALOGPS logs -3.94 ALOGPS solubility 3.30e-02 g/l ALOGPS logp 5.44 ChemAxon pka_strongest_acidic 9.13 ChemAxon pka_strongest_basic -5.7 ChemAxon iupac 2-[(1R,6R)-3-methyl-6-(prop-1-en-2-yl)cyclohex-2-en-1-yl]-5-propylbenzene-1,3-diol ChemAxon average_mass 286.415 ChemAxon mono_mass 286.193280077 ChemAxon smiles [H][C@]1(CCC(C)=C[C@@]1([H])C1=C(O)C=C(CCC)C=C1O)C(C)=C ChemAxon formula C19H26O2 ChemAxon inchi InChI=1S/C19H26O2/c1-5-6-14-10-17(20)19(18(21)11-14)16-9-13(4)7-8-15(16)12(2)3/h9-11,15-16,20-21H,2,5-8H2,1,3-4H3/t15-,16+/m0/s1 ChemAxon inchikey REOZWEGFPHTFEI-JKSUJKDBSA-N ChemAxon polar_surface_area 40.46 ChemAxon refractivity 89.33 ChemAxon polarizability 34.05 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 2 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 103066 Specdb::CMs 103067 Specdb::MsMs 1450613 Specdb::MsMs 1450614 Specdb::MsMs 1450615 Specdb::MsMs 1461470 Specdb::MsMs 1461471 Specdb::MsMs 1461472