1.0 2026-09-22 04:14:44 UTC 2026-09-22 04:14:44 UTC FDB117685 Chlorpyrifos-methyl dimethoxy-sulfanylidene-[(3,5,6-trichloro-2-pyridinyl)oxy]-lambda5-phosphane dimethoxy-thioxo-[(3,5,6-trichloro-2-pyridyl)oxy]-lambda5-phosphane C7H7Cl3NO3PS 322.533 320.894983418 O,O-dimethyl O-3,5,6-trichloropyridin-2-yl phosphorothioate O,O-dimethyl O-3,5,6-trichloropyridin-2-yl phosphorothioate COP(=S)(OC)OC1=NC(Cl)=C(Cl)C=C1Cl InChI=1S/C7H7Cl3NO3PS/c1-12-15(16,13-2)14-7-5(9)3-4(8)6(10)11-7/h3H,1-2H3 HRBKVYFZANMGRE-UHFFFAOYSA-N belongs to the class of organic compounds known as aryl thiophosphates. These are organic compounds containing the thiophosphoric acid functional group or a derivative thereof, with the general structure ROP(OR')(OR'')=S, where at least one R-group is an aryl group. Aryl thiophosphates Organic compounds Organic acids and derivatives Organic thiophosphoric acids and derivatives Thiophosphoric acid esters Aromatic heteromonocyclic compounds 2-halopyridines Aryl chlorides Azacyclic compounds Heteroaromatic compounds Hydrocarbon derivatives Organochlorides Organonitrogen compounds Organooxygen compounds Organopnictogen compounds Polyhalopyridines Thiophosphate triesters 2-halopyridine Aromatic heteromonocyclic compound Aryl chloride Aryl halide Aryl thiophosphate Azacycle Heteroaromatic compound Hydrocarbon derivative Organic nitrogen compound Organic oxygen compound Organochloride Organohalogen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Polyhalopyridine Pyridine Thiophosphate triester Organophosphorus insecticides chloropyridine organic thiophosphate logp 4.30 ALOGPS logs -4.99 ALOGPS solubility 3.33e-03 g/l ALOGPS logp 4.07 ChemAxon pka_strongest_basic -4.2 ChemAxon iupac O,O-dimethyl O-3,5,6-trichloropyridin-2-yl phosphorothioate ChemAxon average_mass 322.533 ChemAxon mono_mass 320.894983418 ChemAxon smiles COP(=S)(OC)OC1=NC(Cl)=C(Cl)C=C1Cl ChemAxon formula C7H7Cl3NO3PS ChemAxon inchi InChI=1S/C7H7Cl3NO3PS/c1-12-15(16,13-2)14-7-5(9)3-4(8)6(10)11-7/h3H,1-2H3 ChemAxon inchikey HRBKVYFZANMGRE-UHFFFAOYSA-N ChemAxon polar_surface_area 40.58 ChemAxon refractivity 69.5 ChemAxon polarizability 26.21 ChemAxon rotatable_bond_count 4 ChemAxon acceptor_count 1 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::NmrOneD 3547 Specdb::NmrOneD 3684 Specdb::CMs 112079 Specdb::CMs 125472 Specdb::EiMs 1490 Specdb::MsMs 105891 Specdb::MsMs 105892 Specdb::MsMs 105893 Specdb::MsMs 172509 Specdb::MsMs 172510 Specdb::MsMs 172511 Specdb::MsMs 2227030 Specdb::MsMs 2227671 Specdb::MsMs 2229394 Specdb::MsMs 2230091 Specdb::MsMs 2234839 Specdb::MsMs 2252930 Specdb::MsMs 2253554 Specdb::MsMs 2255033 Specdb::MsMs 2255530 Specdb::MsMs 2256973 Specdb::MsMs 2257035 Specdb::MsMs 2257582 Specdb::MsMs 2257630 Specdb::MsMs 2259640 Specdb::MsMs 3423749 Specdb::MsMs 3423750 Specdb::MsMs 3423751 Specdb::MsMs 3423752 Specdb::MsMs 3423753