1.0 2010-04-08 22:11:15 UTC 2018-05-29 01:11:50 UTC FDB014410 8,15-Isopimaradien-18-oic acid Found in resin of Pinus subspecies especies Pinus edulis (pinon) (4-Aminophenyl)-onous acid (P-Aminophenyl)-onous acid D8-Isopimaric acid P-Aminobenzeneonous acid P-aminobenzenephosphonous acid Phosphonous acid, (4-aminophenyl)- Phosphonous acid, (p-aminophenyl)- C20H30O2 302.451 302.224580204 7-ethenyl-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid 7-ethenyl-1,4a,7-trimethyl-3,4,5,6,8,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 3625-01-2 CC1(CCC2=C(CCC3C(C)(CCCC23C)C(O)=O)C1)C=C InChI=1S/C20H30O2/c1-5-18(2)12-9-15-14(13-18)7-8-16-19(15,3)10-6-11-20(16,4)17(21)22/h5,16H,1,6-13H2,2-4H3,(H,21,22) BFPAVSSBPLQXJZ-UHFFFAOYSA-N belongs to the class of organic compounds known as diterpenoids. These are terpene compounds formed by four isoprene units. Diterpenoids Organic compounds Lipids and lipid-like molecules Prenol lipids Diterpenoids Aliphatic homopolycyclic compounds Carbonyl compounds Carboxylic acids Hydrocarbon derivatives Hydrophenanthrenes Monocarboxylic acids and derivatives Organic oxides Aliphatic homopolycyclic compound Carbonyl group Carboxylic acid Carboxylic acid derivative Diterpenoid Hydrocarbon derivative Hydrophenanthrene Monocarboxylic acid or derivatives Organic oxide Organic oxygen compound Organooxygen compound Phenanthrene Pimarane diterpenoid logp 4.86 ALOGPS logs -4.94 ALOGPS solubility 3.47e-03 g/l ALOGPS melting_point Mp 105-106° logp 5.02 ChemAxon pka_strongest_acidic 4.8 ChemAxon iupac 7-ethenyl-1,4a,7-trimethyl-1,2,3,4,4a,5,6,7,8,9,10,10a-dodecahydrophenanthrene-1-carboxylic acid ChemAxon average_mass 302.451 ChemAxon mono_mass 302.224580204 ChemAxon smiles CC1(CCC2=C(CCC3C(C)(CCCC23C)C(O)=O)C1)C=C ChemAxon formula C20H30O2 ChemAxon inchi InChI=1S/C20H30O2/c1-5-18(2)12-9-15-14(13-18)7-8-16-19(15,3)10-6-11-20(16,4)17(21)22/h5,16H,1,6-13H2,2-4H3,(H,21,22) ChemAxon inchikey BFPAVSSBPLQXJZ-UHFFFAOYSA-N ChemAxon polar_surface_area 37.3 ChemAxon refractivity 90.07 ChemAxon polarizability 36.08 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 2 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 13136 Specdb::CMs 44508 Specdb::CMs 152908 Specdb::MsMs 6551 Specdb::MsMs 6552 Specdb::MsMs 6553 Specdb::MsMs 13223 Specdb::MsMs 13224 Specdb::MsMs 13225 Specdb::MsMs 2357667 Specdb::MsMs 2357668 Specdb::MsMs 2357669 Specdb::MsMs 2604062 Specdb::MsMs 2604063 Specdb::MsMs 2604064 HMDB35692 #<Reference:0x000055ce31d9ff80>