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CAS 885588-15-8

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Methyl 5-fluoro-2-methyl-4-pyridinecarboxylate

Description:
Methyl 5-fluoro-2-methyl-4-pyridinecarboxylate is an organic compound characterized by its pyridine ring structure, which includes a fluorine atom and a methyl group as substituents. This compound features a carboxylate functional group, indicating its potential for various chemical reactions, including esterification and nucleophilic substitution. The presence of the fluorine atom enhances its reactivity and can influence its biological activity, making it of interest in medicinal chemistry. Methyl 5-fluoro-2-methyl-4-pyridinecarboxylate is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its solubility in organic solvents suggests it can be utilized in various synthetic applications, including the development of pharmaceuticals and agrochemicals. The compound's molecular structure contributes to its unique properties, such as its boiling point, melting point, and reactivity profile, which are essential for understanding its behavior in different chemical environments. Overall, this compound exemplifies the diverse applications of fluorinated pyridine derivatives in modern chemistry.
Formula:C8H8FNO2
InChI:InChI=1S/C8H8FNO2/c1-5-3-6(8(11)12-2)7(9)4-10-5/h3-4H,1-2H3
InChI key:InChIKey=MWNQVBSKYLSQGC-UHFFFAOYSA-N
SMILES:C(OC)(=O)C=1C(F)=CN=C(C)C1
Synonyms:
  • 4-Pyridinecarboxylic acid, 5-fluoro-2-methyl-, methyl ester
  • Methyl 5-fluoro-2-methylisonicotinate
  • Methyl 5-fluoro-2-methyl-4-pyridinecarboxylate
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