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CAS 301666-92-2

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Ethyl 2-chloro-3-methyl-4-pyridinecarboxylate

Description:
Ethyl 2-chloro-3-methyl-4-pyridinecarboxylate is an organic compound characterized by its pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a chloro substituent at the 2-position and a methyl group at the 3-position of the pyridine ring, along with an ethyl ester functional group at the 4-position. The presence of the chloro group introduces reactivity, making it useful in various synthetic applications, particularly in medicinal chemistry and the development of agrochemicals. The ethyl ester moiety contributes to its solubility in organic solvents and can participate in esterification and hydrolysis reactions. Additionally, the compound's structure suggests potential for hydrogen bonding and dipole interactions due to the electronegative chlorine and nitrogen atoms. Its unique combination of functional groups may also impart specific biological activities, making it a candidate for further research in pharmacology. Overall, Ethyl 2-chloro-3-methyl-4-pyridinecarboxylate is a versatile compound with applications in both synthetic and biological chemistry.
Formula:C9H10ClNO2
InChI:InChI=1S/C9H10ClNO2/c1-3-13-9(12)7-4-5-11-8(10)6(7)2/h4-5H,3H2,1-2H3
InChI key:InChIKey=XYEFRKCXSJVAMO-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(C)=C(Cl)N=CC1
Synonyms:
  • 2-Chloro-3-Methylpyridine-4-Carboxylic Acid Ethyl Ester
  • 4-Pyridinecarboxylic acid, 2-chloro-3-methyl-, ethyl ester
  • Ethyl 2-Chloro-3-Methylpyridine-4-Carboxylate
  • Ethyl 2-chloro-3-methyl-4-pyridinecarboxylate
  • Ethyl 2-chloro-3-methylisonicotinate
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