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CAS 603122-76-5

:

ethyl 2,5-dichloropyridine-4-carboxylate

Description:
Ethyl 2,5-dichloropyridine-4-carboxylate is an organic compound characterized by its pyridine ring, which is substituted at the 2 and 5 positions with chlorine atoms and at the 4 position with a carboxylate group. This compound features an ethyl ester functional group, contributing to its reactivity and solubility properties. Typically, it appears as a colorless to pale yellow liquid or solid, depending on its purity and form. Ethyl 2,5-dichloropyridine-4-carboxylate is known for its applications in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to the presence of the pyridine moiety, which is a common scaffold in many biologically active compounds. The dichlorination enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. Safety data should be consulted, as halogenated compounds can pose environmental and health risks. Overall, this compound exemplifies the diverse utility of halogenated heterocycles in modern chemistry.
Formula:C8H7Cl2NO2
InChI:InChI=1/C8H7Cl2NO2/c1-2-13-8(12)5-3-7(10)11-4-6(5)9/h3-4H,2H2,1H3
SMILES:CCOC(=O)c1cc(Cl)ncc1Cl
Synonyms:
  • 4-Pyridinecarboxylic Acid, 2,5-Dichloro-, Ethyl Ester
  • Ethyl 2,5-dichloroisonicotinate
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