1.0 2026-09-22 05:39:56 UTC 2026-09-22 05:39:56 UTC FDB117781 Thifluzamide N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-1,3-thiazole-5-carboxamide N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)thiazole-5-carboxamide C13H6Br2F6N2O2S 528.06 525.842094 N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-1,3-thiazole-5-carboximidic acid N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-1,3-thiazole-5-carboximidic acid CC1=NC(=C(S1)C(O)=NC1=C(Br)C=C(OC(F)(F)F)C=C1Br)C(F)(F)F InChI=1S/C13H6Br2F6N2O2S/c1-4-22-10(12(16,17)18)9(26-4)11(24)23-8-6(14)2-5(3-7(8)15)25-13(19,20)21/h2-3H,1H3,(H,23,24) WOSNCVAPUOFXEH-UHFFFAOYSA-N belongs to the class of organic compounds known as 2,4,5-trisubstituted thiazoles. 2,4,5-trisubstituted thiazoles are compounds containing a thiazole ring substituted at positions 2, 4 and 5 only. 2,4,5-trisubstituted thiazoles Organic compounds Organoheterocyclic compounds Azoles Thiazoles Aromatic heteromonocyclic compounds Alkyl fluorides Aryl bromides Azacyclic compounds Bromobenzenes Carboximidic acids Heteroaromatic compounds Hydrocarbon derivatives Organobromides Organofluorides Organonitrogen compounds Organooxygen compounds Organopnictogen compounds Phenol ethers Phenoxy compounds Propargyl-type 1,3-dipolar organic compounds Trihalomethanes 2,4,5-trisubstituted 1,3-thiazole Alkyl fluoride Alkyl halide Aromatic heteromonocyclic compound Aryl bromide Aryl halide Azacycle Benzenoid Bromobenzene Carboximidic acid Carboximidic acid derivative Halobenzene Halomethane Heteroaromatic compound Hydrocarbon derivative Monocyclic benzene moiety Organic 1,3-dipolar compound Organic nitrogen compound Organic oxygen compound Organobromide Organofluoride Organohalogen compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenol ether Phenoxy compound Propargyl-type 1,3-dipolar organic compound Trihalomethane 1,3-thiazole Thiazole fungicides anilide fungicide aromatic amide aromatic ether dibromobenzene organofluorine compound logp 5.17 ALOGPS logs -5.75 ALOGPS solubility 9.30e-04 g/l ALOGPS logp 6.26 ChemAxon pka_strongest_acidic -0.9 ChemAxon pka_strongest_basic 1.19 ChemAxon iupac N-[2,6-dibromo-4-(trifluoromethoxy)phenyl]-2-methyl-4-(trifluoromethyl)-1,3-thiazole-5-carboximidic acid ChemAxon average_mass 528.06 ChemAxon mono_mass 525.842094 ChemAxon smiles CC1=NC(=C(S1)C(O)=NC1=C(Br)C=C(OC(F)(F)F)C=C1Br)C(F)(F)F ChemAxon formula C13H6Br2F6N2O2S ChemAxon inchi InChI=1S/C13H6Br2F6N2O2S/c1-4-22-10(12(16,17)18)9(26-4)11(24)23-8-6(14)2-5(3-7(8)15)25-13(19,20)21/h2-3H,1H3,(H,23,24) ChemAxon inchikey WOSNCVAPUOFXEH-UHFFFAOYSA-N ChemAxon polar_surface_area 54.71 ChemAxon refractivity 85.7 ChemAxon polarizability 34.95 ChemAxon rotatable_bond_count 5 ChemAxon acceptor_count 4 ChemAxon donor_count 1 ChemAxon physiological_charge -1 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 44628 Specdb::MsMs 44629 Specdb::MsMs 44630 Specdb::MsMs 150738 Specdb::MsMs 150739 Specdb::MsMs 150740