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CAS 1000340-08-8

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Ethyl 5-fluoro-1,6-dihydro-4-hydroxy-6-oxo-3-pyridinecarboxylate

Description:
Ethyl 5-fluoro-1,6-dihydro-4-hydroxy-6-oxo-3-pyridinecarboxylate is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a fluorine substituent at the 5-position, contributing to its unique reactivity and potential biological activity. The presence of a carboxylate group indicates that it can participate in various chemical reactions, including esterification and nucleophilic substitutions. The hydroxyl group at the 4-position enhances its solubility in polar solvents and may influence its interaction with biological targets. Additionally, the 6-oxo group suggests that it may exhibit keto-enol tautomerism, which can affect its stability and reactivity. Ethyl 5-fluoro-1,6-dihydro-4-hydroxy-6-oxo-3-pyridinecarboxylate may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential biological activities. However, specific properties such as melting point, boiling point, and solubility would require empirical data for precise characterization.
Formula:C8H8FNO4
InChI:InChI=1S/C8H8FNO4/c1-2-14-8(13)4-3-10-7(12)5(9)6(4)11/h3H,2H2,1H3,(H2,10,11,12)
InChI key:InChIKey=KRPFLIYEGCRSFO-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(O)=C(F)C(=O)NC1
Synonyms:
  • Ethyl 5-fluoro-1,6-dihydro-4-hydroxy-6-oxo-3-pyridinecarboxylate
  • 3-Pyridinecarboxylic acid, 5-fluoro-1,6-dihydro-4-hydroxy-6-oxo-, ethyl ester
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