1.0 2026-09-22 20:46:36 UTC 2026-09-22 20:46:36 UTC FDB118853 pyridalyl 2-[3-[2,6-dichloro-4-(3,3-dichloroallyloxy)phenoxy]propoxy]-5-(trifluoromethyl)pyridine 2-[3-[2,6-dichloro-4-(3,3-dichloroprop-2-enoxy)phenoxy]propoxy]-5-(trifluoromethyl)pyridine C18H14Cl4F3NO3 491.11 488.9679886 2-(3-{2,6-dichloro-4-[(3,3-dichloroprop-2-en-1-yl)oxy]phenoxy}propoxy)-5-(trifluoromethyl)pyridine pyridalyl FC(F)(F)C1=CN=C(OCCCOC2=C(Cl)C=C(OCC=C(Cl)Cl)C=C2Cl)C=C1 InChI=1S/C18H14Cl4F3NO3/c19-13-8-12(27-7-4-15(21)22)9-14(20)17(13)29-6-1-5-28-16-3-2-11(10-26-16)18(23,24)25/h2-4,8-10H,1,5-7H2 AEHJMNVBLRLZKK-UHFFFAOYSA-N belongs to the class of organic compounds known as dichlorobenzenes. Dichlorobenzenes are compounds containing a benzene with exactly two chlorine atoms attached to it. Dichlorobenzenes Organic compounds Benzenoids Benzene and substituted derivatives Halobenzenes Aromatic heteromonocyclic compounds Alkyl aryl ethers Alkyl fluorides Aryl chlorides Azacyclic compounds Chloroalkenes Heteroaromatic compounds Hydrocarbon derivatives Ketene acetals Organochlorides Organofluorides Organonitrogen compounds Organopnictogen compounds Phenol ethers Phenoxy compounds Pyridines and derivatives Vinyl chlorides 1,3-dichlorobenzene Alkyl aryl ether Alkyl fluoride Alkyl halide Aromatic heteromonocyclic compound Aryl chloride Aryl halide Azacycle Chloroalkene Ether Haloalkene Heteroaromatic compound Hydrocarbon derivative Ketene acetal or derivatives Organic nitrogen compound Organic oxygen compound Organochloride Organofluoride Organohalogen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenol ether Phenoxy compound Pyridine Vinyl chloride Vinyl halide dichlorobenzene organochlorine insecticide organofluorine insecticide logp 6.40 ALOGPS logs -6.20 ALOGPS solubility 3.13e-04 g/l ALOGPS logp 6.31 ChemAxon pka_strongest_basic 1.75 ChemAxon iupac 2-(3-{2,6-dichloro-4-[(3,3-dichloroprop-2-en-1-yl)oxy]phenoxy}propoxy)-5-(trifluoromethyl)pyridine ChemAxon average_mass 491.11 ChemAxon mono_mass 488.9679886 ChemAxon smiles FC(F)(F)C1=CN=C(OCCCOC2=C(Cl)C=C(OCC=C(Cl)Cl)C=C2Cl)C=C1 ChemAxon formula C18H14Cl4F3NO3 ChemAxon inchi InChI=1S/C18H14Cl4F3NO3/c19-13-8-12(27-7-4-15(21)22)9-14(20)17(13)29-6-1-5-28-16-3-2-11(10-26-16)18(23,24)25/h2-4,8-10H,1,5-7H2 ChemAxon inchikey AEHJMNVBLRLZKK-UHFFFAOYSA-N ChemAxon polar_surface_area 40.58 ChemAxon refractivity 117.7 ChemAxon polarizability 43 ChemAxon rotatable_bond_count 10 ChemAxon acceptor_count 4 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 1326022 Specdb::MsMs 1326023 Specdb::MsMs 1326024 Specdb::MsMs 1440373 Specdb::MsMs 1440374 Specdb::MsMs 1440375