1.0 2026-09-22 16:39:37 UTC 2026-09-22 16:39:37 UTC FDB118536 Prochloraz N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]imidazole-1-carboxamide C15H16Cl3N3O2 376.665 375.030809892 N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]-1H-imidazole-1-carboxamide prochloraz CCCN(CCOC1=C(Cl)C=C(Cl)C=C1Cl)C(=O)N1C=CN=C1 InChI=1S/C15H16Cl3N3O2/c1-2-4-20(15(22)21-5-3-19-10-21)6-7-23-14-12(17)8-11(16)9-13(14)18/h3,5,8-10H,2,4,6-7H2,1H3 TVLSRXXIMLFWEO-UHFFFAOYSA-N belongs to the class of organic compounds known as phenol ethers. These are aromatic compounds containing an ether group substituted with a benzene ring. Phenol ethers Organic compounds Benzenoids Phenol ethers Aromatic heteromonocyclic compounds Alkyl aryl ethers Aryl chlorides Azacyclic compounds Carbonylimidazoles Chlorobenzenes Heteroaromatic compounds Hydrocarbon derivatives N-substituted imidazoles Organic oxides Organochlorides Organonitrogen compounds Organopnictogen compounds Phenoxy compounds Ureas Alkyl aryl ether Aromatic heteromonocyclic compound Aryl chloride Aryl halide Azacycle Azole Carbonic acid derivative Chlorobenzene Ether Halobenzene Heteroaromatic compound Hydrocarbon derivative Imidazole Imidazole-1-carbonyl group Monocyclic benzene moiety N-substituted imidazole Organic nitrogen compound Organic oxide Organic oxygen compound Organochloride Organohalogen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenol ether Phenoxy compound Urea Amide fungicides amide fungicide aromatic ether conazole fungicide imidazole fungicide imidazoles trichlorobenzene ureas logp 3.78 ALOGPS logs -4.62 ALOGPS solubility 9.10e-03 g/l ALOGPS logp 3.62 ChemAxon pka_strongest_basic 2.75 ChemAxon iupac N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]-1H-imidazole-1-carboxamide ChemAxon average_mass 376.665 ChemAxon mono_mass 375.030809892 ChemAxon smiles CCCN(CCOC1=C(Cl)C=C(Cl)C=C1Cl)C(=O)N1C=CN=C1 ChemAxon formula C15H16Cl3N3O2 ChemAxon inchi InChI=1S/C15H16Cl3N3O2/c1-2-4-20(15(22)21-5-3-19-10-21)6-7-23-14-12(17)8-11(16)9-13(14)18/h3,5,8-10H,2,4,6-7H2,1H3 ChemAxon inchikey TVLSRXXIMLFWEO-UHFFFAOYSA-N ChemAxon polar_surface_area 47.36 ChemAxon refractivity 90.99 ChemAxon polarizability 35.73 ChemAxon rotatable_bond_count 6 ChemAxon acceptor_count 3 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::NmrOneD 3564 Specdb::NmrOneD 3699 Specdb::EiMs 1506 Specdb::CMs 34974 Specdb::CMs 160503 Specdb::MsMs 107487 Specdb::MsMs 107488 Specdb::MsMs 107489 Specdb::MsMs 174477 Specdb::MsMs 174478 Specdb::MsMs 174479 Specdb::MsMs 441482 Specdb::MsMs 441483 Specdb::MsMs 441484 Specdb::MsMs 441485 Specdb::MsMs 441486 Specdb::MsMs 441487 Specdb::MsMs 441488 Specdb::MsMs 441489 Specdb::MsMs 441490 Specdb::MsMs 441491 Specdb::MsMs 441492 Specdb::MsMs 441493 Specdb::MsMs 441494 Specdb::MsMs 441495 Specdb::MsMs 448878 Specdb::MsMs 448879 Specdb::MsMs 452329 Specdb::MsMs 452582 Specdb::MsMs 452583