1.0 2026-09-22 05:51:03 UTC 2026-09-22 05:51:03 UTC FDB117793 Clodinafop-Propargyl prop-2-ynyl (2R)-2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]propanoate prop-2-ynyl (2R)-2-[4-[(5-chloro-3-fluoro-2-pyridyl)oxy]phenoxy]propanoate C17H13ClFNO4 349.741 349.051713821 prop-2-yn-1-yl (2R)-2-{4-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenoxy}propanoate prop-2-yn-1-yl (2R)-2-{4-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenoxy}propanoate [H][C@](C)(OC1=CC=C(OC2=C(F)C=C(Cl)C=N2)C=C1)C(=O)OCC#C InChI=1S/C17H13ClFNO4/c1-3-8-22-17(21)11(2)23-13-4-6-14(7-5-13)24-16-15(19)9-12(18)10-20-16/h1,4-7,9-11H,8H2,2H3/t11-/m1/s1 JBDHZKLJNAIJNC-LLVKDONJSA-N belongs to the class of organic compounds known as 2-phenoxypropionic acid esters. These are aromatic compounds hat contain a phenol ether attached to the C2-atom of a phenylpropionic acid ester. 2-phenoxypropionic acid esters Organic compounds Benzenoids Benzene and substituted derivatives 2-phenoxypropionic acid esters Aromatic heteromonocyclic compounds Acetylides Alkyl aryl ethers Aryl chlorides Aryl fluorides Azacyclic compounds Carbonyl compounds Carboxylic acid esters Diarylethers Heteroaromatic compounds Hydrocarbon derivatives Monocarboxylic acids and derivatives Organic oxides Organochlorides Organofluorides Organonitrogen compounds Organopnictogen compounds Phenol ethers Phenoxy compounds Phenoxyacetic acid derivatives Polyhalopyridines 2-phenoxypropionic acid ester Acetylide Alkyl aryl ether Aromatic heteromonocyclic compound Aryl chloride Aryl fluoride Aryl halide Azacycle Carbonyl group Carboxylic acid derivative Carboxylic acid ester Diaryl ether Ether Heteroaromatic compound Hydrocarbon derivative Monocarboxylic acid or derivatives Organic nitrogen compound Organic oxide Organic oxygen compound Organochloride Organofluoride Organohalogen compound Organoheterocyclic compound Organonitrogen compound Organooxygen compound Organopnictogen compound Phenol ether Phenoxy compound Phenoxyacetate Polyhalopyridine Pyridine logp 3.68 ALOGPS logs -4.74 ALOGPS solubility 6.35e-03 g/l ALOGPS logp 3.86 ChemAxon pka_strongest_basic -2.2 ChemAxon iupac prop-2-yn-1-yl (2R)-2-{4-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenoxy}propanoate ChemAxon average_mass 349.741 ChemAxon mono_mass 349.051713821 ChemAxon smiles [H][C@](C)(OC1=CC=C(OC2=C(F)C=C(Cl)C=N2)C=C1)C(=O)OCC#C ChemAxon formula C17H13ClFNO4 ChemAxon inchi InChI=1S/C17H13ClFNO4/c1-3-8-22-17(21)11(2)23-13-4-6-14(7-5-13)24-16-15(19)9-12(18)10-20-16/h1,4-7,9-11H,8H2,2H3/t11-/m1/s1 ChemAxon inchikey JBDHZKLJNAIJNC-LLVKDONJSA-N ChemAxon polar_surface_area 57.65 ChemAxon refractivity 84.87 ChemAxon polarizability 32.68 ChemAxon rotatable_bond_count 7 ChemAxon acceptor_count 3 ChemAxon donor_count 0 ChemAxon physiological_charge 0 ChemAxon formal_charge 0 ChemAxon Specdb::MsMs 107550 Specdb::MsMs 107551 Specdb::MsMs 107552 Specdb::MsMs 174546 Specdb::MsMs 174547 Specdb::MsMs 174548