1.0 2010-04-08 22:14:56 UTC 2018-05-28 19:58:33 UTC FDB020316 Pyriminobac-methyl Herbicide used on rice E-pyriminobac-methyl KIH 6127 KUH 920 Prosper Pyriminobac-methyl [iso:bsi] Pyriminobac-methyl [iso] Pyriminobac-methyl, BSI C17H19N3O6 361.3493 361.127385355 methyl 2-[(4,6-dimethoxypyrimidin-2-yl)oxy]-6-[(1E)-1-(methoxyimino)ethyl]benzoate pyriminobac-methyl 136191-64-5 CO\N=C(/C)C1=C(C(=O)OC)C(OC2=NC(OC)=CC(OC)=N2)=CC=C1 InChI=1S/C17H19N3O6/c1-10(20-25-5)11-7-6-8-12(15(11)16(21)24-4)26-17-18-13(22-2)9-14(19-17)23-3/h6-9H,1-5H3/b20-10+ USSIUIGPBLPCDF-KEBDBYFISA-N belongs to the class of organic compounds known as diarylethers. These are organic compounds containing the dialkyl ether functional group, with the formula ROR', where R and R' are aryl groups. Diarylethers Organic compounds Organic oxygen compounds Organooxygen compounds Ethers Aromatic heteromonocyclic compounds Alkyl aryl ethers Azacyclic compounds Benzoic acid esters Benzoyl derivatives Heteroaromatic compounds Hydrocarbon derivatives Methyl esters Monocarboxylic acids and derivatives Organic oxides Organonitrogen compounds Organopnictogen compounds Phenol ethers Phenoxy compounds Pyrimidines and pyrimidine derivatives Alkyl aryl ether Aromatic heteromonocyclic compound Azacycle Benzenoid Benzoate ester Benzoic acid or derivatives Benzoyl Carboxylic acid derivative Carboxylic acid ester Diaryl ether Heteroaromatic compound Hydrocarbon derivative Methyl ester Monocarboxylic acid or derivatives Monocyclic benzene moiety Organic nitrogen compound Organic oxide Organoheterocyclic compound Organonitrogen compound Organopnictogen compound Phenol ether Phenoxy compound Pyrimidine Benzoic acid herbicides aromatic ether logp 2.87 ALOGPS logs -3.69 ALOGPS solubility 7.38e-02 g/l ALOGPS melting_point Mp 105-106° logp 3.05 ChemAxon pka_strongest_basic 1.49 ChemAxon iupac methyl 2-[(4,6-dimethoxypyrimidin-2-yl)oxy]-6-[(1E)-1-(methoxyimino)ethyl]benzoate ChemAxon average_mass 361.3493 ChemAxon mono_mass 361.127385355 ChemAxon smiles CO\N=C(/C)C1=C(C(=O)OC)C(OC2=NC(OC)=CC(OC)=N2)=CC=C1 ChemAxon formula C17H19N3O6 ChemAxon inchi InChI=1S/C17H19N3O6/c1-10(20-25-5)11-7-6-8-12(15(11)16(21)24-4)26-17-18-13(22-2)9-14(19-17)23-3/h6-9H,1-5H3/b20-10+ ChemAxon inchikey USSIUIGPBLPCDF-KEBDBYFISA-N ChemAxon polar_surface_area 101.36 ChemAxon refractivity 93.19 ChemAxon polarizability 35.54 ChemAxon rotatable_bond_count 8 ChemAxon acceptor_count 7 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::CMs 14896 Specdb::CMs 153989 Specdb::MsMs 56580 Specdb::MsMs 56581 Specdb::MsMs 56582 Specdb::MsMs 112029 Specdb::MsMs 112030 Specdb::MsMs 112031 Specdb::MsMs 2399571 Specdb::MsMs 2399572 Specdb::MsMs 2399573 Specdb::MsMs 2536619 Specdb::MsMs 2536620 Specdb::MsMs 2536621 HMDB40546 #<Reference:0x000055ce31885590>