1.0 2010-04-08 22:12:15 UTC 2015-07-20 23:25:44 UTC FDB016125 (±)-Furilazole Herbicide safener for gramineous crops (RS)-3-dichloroacetyl-5-(2-furanyl)-2,2-dimethyloxazolidine 3-(Dichloroacetyl)-5-(2-furanyl)-2,2-dimethyl-oxazolidine 3-(dichloroacetyl)-5-(2-furanyl)-2,2-dimethyloxazolidine Furilazole Nanogen Index Code FUA (3-010) Oxazolidine, 3-(dichloroacetyl)-5-(2-furanyl)-2,2-dimethyl- C11H13Cl2NO3 278.132 277.027248701 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethan-1-one furilazole 141980-03-2 CC1(C)OC(CN1C(=O)C(Cl)Cl)C1=CC=CO1 InChI=1S/C11H13Cl2NO3/c1-11(2)14(10(15)9(12)13)6-8(17-11)7-4-3-5-16-7/h3-5,8-9H,6H2,1-2H3 MCNOFYBITGAAGM-UHFFFAOYSA-N belongs to the class of organic compounds known as oxazolidines. Oxazolidines are compounds containing an oxazolidine moiety, which consists of a saturated aliphatic five-member ring with one oxygen atom, one nitrogen, three carbon atoms, and two double bonds. Oxazolidines Organic compounds Organoheterocyclic compounds Azolidines Oxazolidines Aromatic heteromonocyclic compounds Alkyl chlorides Azacyclic compounds Carbonyl compounds Furans Heteroaromatic compounds Hydrocarbon derivatives Organic oxides Organochlorides Organonitrogen compounds Organopnictogen compounds Oxacyclic compounds Tertiary carboxylic acid amides Alkyl chloride Alkyl halide Aromatic heteromonocyclic compound Azacycle Carbonyl group Carboxamide group Carboxylic acid derivative Furan Heteroaromatic compound Hydrocarbon derivative Organic nitrogen compound Organic oxide Organic oxygen compound Organochloride Organohalogen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Oxacycle Oxazolidine Tertiary carboxylic acid amide logp 2.44 ALOGPS logs -3.12 ALOGPS solubility 2.11e-01 g/l ALOGPS melting_point Mp 97-98° logp 1.91 ChemAxon pka_strongest_acidic 16.45 ChemAxon pka_strongest_basic -3.4 ChemAxon iupac 2,2-dichloro-1-[5-(furan-2-yl)-2,2-dimethyl-1,3-oxazolidin-3-yl]ethan-1-one ChemAxon average_mass 278.132 ChemAxon mono_mass 277.027248701 ChemAxon smiles CC1(C)OC(CN1C(=O)C(Cl)Cl)C1=CC=CO1 ChemAxon formula C11H13Cl2NO3 ChemAxon inchi InChI=1S/C11H13Cl2NO3/c1-11(2)14(10(15)9(12)13)6-8(17-11)7-4-3-5-16-7/h3-5,8-9H,6H2,1-2H3 ChemAxon inchikey MCNOFYBITGAAGM-UHFFFAOYSA-N ChemAxon polar_surface_area 42.68 ChemAxon refractivity 64.66 ChemAxon polarizability 26.38 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 2 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 23189 Specdb::MsMs 43704 Specdb::MsMs 43705 Specdb::MsMs 43706 Specdb::MsMs 116616 Specdb::MsMs 116617 Specdb::MsMs 116618 HMDB37131 #<Reference:0x000055ce307c5048>