1.0 2010-04-08 22:12:45 UTC 2015-07-20 23:34:19 UTC FDB016955 4,11-Dichloro-5,12-dihydroquino[2,3-b]acridine-7,14-dione FDA approved colourant for food contact polymers 4,11 DCQA 4,11-dichloro quinacridone 4,11-Dichloro-5,12-dihydroquino(2,3-b)acridine-7,14-dione 4,11-Dichloro-quinacridone Quinacridone, 4,11-dichloro- C20H10Cl2N2O2 381.212 380.011932988 4,11-dichloro-5,7,12,14-tetrahydro-5,12-diazapentacene-7,14-dione 4,11-dichloro-5,12-dihydro-5,12-diazapentacene-7,14-dione 3089-16-5 ClC1=CC=CC2=C1NC1=CC3=C(NC4=C(C=CC=C4Cl)C3=O)C=C1C2=O InChI=1S/C20H10Cl2N2O2/c21-13-5-1-3-9-17(13)23-15-8-12-16(7-11(15)19(9)25)24-18-10(20(12)26)4-2-6-14(18)22/h1-8H,(H,23,25)(H,24,26) BFEJTCHFLJECJN-UHFFFAOYSA-N belongs to the class of organic compounds known as pyridoacridines. Pyridoacridines are compounds containing a pyridoacridine ring system, which consists of a pyridine fused to an acridine. Pyridoacridines Organic compounds Organoheterocyclic compounds Quinolines and derivatives Benzoquinolines Aromatic heteropolycyclic compounds Acridones Aryl chlorides Azacyclic compounds Benzenoids Chloroquinolines Heteroaromatic compounds Hydrocarbon derivatives Hydroquinolines Hydroquinolones Organic oxides Organochlorides Organonitrogen compounds Organooxygen compounds Organopnictogen compounds Pyridines and derivatives Vinylogous amides Acridone Aromatic heteropolycyclic compound Aryl chloride Aryl halide Azacycle Benzenoid Chloroquinoline Dihydroquinoline Dihydroquinolone Haloquinoline Heteroaromatic compound Hydrocarbon derivative Organic nitrogen compound Organic oxide Organic oxygen compound Organochloride Organohalogen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Pyridine Pyridoacridine Vinylogous amide logp 5.19 ALOGPS logs -4.88 ALOGPS solubility 5.03e-03 g/l ALOGPS logp 7.63 ChemAxon pka_strongest_acidic 15.28 ChemAxon pka_strongest_basic -3.5 ChemAxon iupac 4,11-dichloro-5,7,12,14-tetrahydro-5,12-diazapentacene-7,14-dione ChemAxon average_mass 381.212 ChemAxon mono_mass 380.011932988 ChemAxon smiles ClC1=CC=CC2=C1NC1=CC3=C(NC4=C(C=CC=C4Cl)C3=O)C=C1C2=O ChemAxon formula C20H10Cl2N2O2 ChemAxon inchi InChI=1S/C20H10Cl2N2O2/c21-13-5-1-3-9-17(13)23-15-8-12-16(7-11(15)19(9)25)24-18-10(20(12)26)4-2-6-14(18)22/h1-8H,(H,23,25)(H,24,26) ChemAxon inchikey BFEJTCHFLJECJN-UHFFFAOYSA-N ChemAxon polar_surface_area 58.2 ChemAxon refractivity 101.68 ChemAxon polarizability 38.06 ChemAxon rotatable_bond_count 0 ChemAxon acceptor_count 4 ChemAxon donor_count 2 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 12100 Specdb::CMs 150364 Specdb::MsMs 105246 Specdb::MsMs 105247 Specdb::MsMs 105248 Specdb::MsMs 171708 Specdb::MsMs 171709 Specdb::MsMs 171710 Specdb::MsMs 2703917 Specdb::MsMs 2703918 Specdb::MsMs 2703919 Specdb::MsMs 3001915 Specdb::MsMs 3001916 Specdb::MsMs 3001917 HMDB37810 #<Reference:0x000055ce31995160>