1.0 2010-04-08 22:09:40 UTC 2018-05-28 23:30:29 UTC FDB011470 (R)-Rhazinilam Alkaloidal artifact from Aspidosperma quebracho-blanco (quebracho). (-)-Rhazinilam Rhazinilam C19H22N2O 294.3908 294.173213336 (8E)-12-ethyl-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(19),2,4,6,8,17-hexaen-9-ol (8E)-12-ethyl-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(19),2,4,6,8,17-hexaen-9-ol 36193-36-9 CCC12CCCN3C=CC(=C13)C1=CC=CC=C1\N=C(O)/CC2 InChI=1S/C19H22N2O/c1-2-19-10-5-12-21-13-9-15(18(19)21)14-6-3-4-7-16(14)20-17(22)8-11-19/h3-4,6-7,9,13H,2,5,8,10-12H2,1H3,(H,20,22) VLQAFTDOIRUYSZ-UHFFFAOYSA-N belongs to the class of organic compounds known as benzenoids. These are aromatic compounds containing one or more benzene rings. Benzenoids Organic compounds Benzenoids Aromatic heteropolycyclic compounds Azacyclic compounds Carbonyl compounds Heteroaromatic compounds Hydrocarbon derivatives Lactams Organic oxides Organonitrogen compounds Organopnictogen compounds Pyrroles Secondary carboxylic acid amides Aromatic heteropolycyclic compound Azacycle Benzenoid Carbonyl group Carboxamide group Carboxylic acid derivative Heteroaromatic compound Hydrocarbon derivative Lactam Organic nitrogen compound Organic oxide Organic oxygen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Pyrrole Secondary carboxylic acid amide logp 4.05 ALOGPS logs -4.04 ALOGPS solubility 2.70e-02 g/l ALOGPS melting_point Mp 214-216° logp 4.56 ChemAxon pka_strongest_acidic 7.63 ChemAxon pka_strongest_basic 0.93 ChemAxon iupac (8E)-12-ethyl-8,16-diazatetracyclo[10.6.1.0²,⁷.0¹⁶,¹⁹]nonadeca-1(19),2,4,6,8,17-hexaen-9-ol ChemAxon average_mass 294.3908 ChemAxon mono_mass 294.173213336 ChemAxon smiles CCC12CCCN3C=CC(=C13)C1=CC=CC=C1\N=C(O)/CC2 ChemAxon formula C19H22N2O ChemAxon inchi InChI=1S/C19H22N2O/c1-2-19-10-5-12-21-13-9-15(18(19)21)14-6-3-4-7-16(14)20-17(22)8-11-19/h3-4,6-7,9,13H,2,5,8,10-12H2,1H3,(H,20,22) ChemAxon inchikey VLQAFTDOIRUYSZ-UHFFFAOYSA-N ChemAxon polar_surface_area 37.52 ChemAxon refractivity 90.71 ChemAxon polarizability 33.35 ChemAxon rotatable_bond_count 1 ChemAxon acceptor_count 2 ChemAxon donor_count 1 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 18012 Specdb::CMs 43289 Specdb::CMs 171727 Specdb::MsMs 6899 Specdb::MsMs 6900 Specdb::MsMs 6901 Specdb::MsMs 13571 Specdb::MsMs 13572 Specdb::MsMs 13573 Specdb::MsMs 2453740 Specdb::MsMs 2453741 Specdb::MsMs 2453742 Specdb::MsMs 2484834 Specdb::MsMs 2484835 Specdb::MsMs 2484836 HMDB33432 #<Reference:0x000055ce32587b08>