1.0 2026-09-22 06:03:06 UTC 2026-09-22 06:03:06 UTC FDB117809 Thiacloprid [3-[(6-chloro-3-pyridinyl)methyl]-1,3-thiazolidin-2-ylidene]cyanamide [3-[(6-chloro-3-pyridyl)methyl]thiazolidin-2-ylidene]cyanamide C10H9ClN4S 252.723 252.023644705 {[(2Z)-3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene]amino}formonitrile {[(2Z)-3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene]amino}formonitrile ClC1=NC=C(CN2CCS\C2=N/C#N)C=C1 InChI=1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2/b14-10- HOKKPVIRMVDYPB-UVTDQMKNSA-N belongs to the class of organic compounds known as 2-halopyridines. These are organic compounds containing a pyridine ring substituted at the 2-position by a halogen atom. 2-halopyridines Organic compounds Organoheterocyclic compounds Pyridines and derivatives Halopyridines Aromatic heteromonocyclic compounds Aryl chlorides Azacyclic compounds Carboximidamides Heteroaromatic compounds Hydrocarbon derivatives Imines Isothioureas Organochlorides Organopnictogen compounds Propargyl-type 1,3-dipolar organic compounds Thiazolidines 2-halopyridine Aromatic heteromonocyclic compound Aryl chloride Aryl halide Azacycle Carboximidamide Heteroaromatic compound Hydrocarbon derivative Imine Isothiourea Organic 1,3-dipolar compound Organic nitrogen compound Organochloride Organohalogen compound Organonitrogen compound Organopnictogen compound Propargyl-type 1,3-dipolar organic compound Thiazolidine Neonicotinoid insecticides thiacloprid logp 1.91 ALOGPS logs -2.74 ALOGPS solubility 4.58e-01 g/l ALOGPS logp 2.06 ChemAxon pka_strongest_basic 1.62 ChemAxon iupac {[(2Z)-3-[(6-chloropyridin-3-yl)methyl]-1,3-thiazolidin-2-ylidene]amino}formonitrile ChemAxon average_mass 252.723 ChemAxon mono_mass 252.023644705 ChemAxon smiles ClC1=NC=C(CN2CCS\C2=N/C#N)C=C1 ChemAxon formula C10H9ClN4S ChemAxon inchi InChI=1S/C10H9ClN4S/c11-9-2-1-8(5-13-9)6-15-3-4-16-10(15)14-7-12/h1-2,5H,3-4,6H2/b14-10- ChemAxon inchikey HOKKPVIRMVDYPB-UVTDQMKNSA-N ChemAxon polar_surface_area 52.28 ChemAxon refractivity 67.05 ChemAxon polarizability 24.48 ChemAxon rotatable_bond_count 2 ChemAxon acceptor_count 4 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 52872 Specdb::MsMs 52873 Specdb::MsMs 52874 Specdb::MsMs 176751 Specdb::MsMs 176752 Specdb::MsMs 176753