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CAS 154012-17-6

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Ethyl 4,6-dichloro-5-fluoro-3-pyridinecarboxylate

Description:
Ethyl 4,6-dichloro-5-fluoro-3-pyridinecarboxylate is a chemical compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing nitrogen. The presence of multiple halogen substituents, specifically two chlorine atoms and one fluorine atom, contributes to its reactivity and potential applications in various chemical reactions. The ethyl ester functional group enhances its solubility in organic solvents, making it useful in synthetic organic chemistry. This compound may exhibit biological activity, which is often explored in pharmaceutical research, particularly in the development of agrochemicals or medicinal compounds. Its molecular structure suggests that it could participate in nucleophilic substitution reactions due to the electrophilic nature of the carbonyl carbon in the carboxylate group. Additionally, the presence of halogens can influence the compound's electronic properties, potentially affecting its interaction with biological targets. Overall, Ethyl 4,6-dichloro-5-fluoro-3-pyridinecarboxylate is a versatile compound with significant implications in both synthetic and applied chemistry.
Formula:C8H6Cl2FNO2
InChI:InChI=1S/C8H6Cl2FNO2/c1-2-14-8(13)4-3-12-7(10)6(11)5(4)9/h3H,2H2,1H3
InChI key:InChIKey=PJAYGSDXQHYXNZ-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(Cl)=C(F)C(Cl)=NC1
Synonyms:
  • 3-Pyridinecarboxylic acid, 4,6-dichloro-5-fluoro-, ethyl ester
  • Ethyl 4,6-dichloro-5-fluoronicotinate
  • Ethyl 4,6-dichloro-5-fluoro-3-pyridinecarboxylate
  • Ethyl 4,6-dichloro-5-fluoropyridine-3-carboxylate, 2,4-Dichloro-5-(ethoxycarbonyl)-3-fluoropyridine
  • ethyl 4,6-dichloro-5-fluoropyridine-3-carboxylate
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