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CAS 186593-48-6

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2-Fluoro-3-methyl-5-aminopyridine

Description:
2-Fluoro-3-methyl-5-aminopyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a fluorine atom at the second position, a methyl group at the third position, and an amino group at the fifth position contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the amino group, which can engage in hydrogen bonding. Its structure suggests potential reactivity in nucleophilic substitution reactions, particularly due to the electron-withdrawing nature of the fluorine atom. Additionally, the amino group can participate in various chemical transformations, making it a valuable intermediate in organic synthesis. The compound may also exhibit biological activity, which is of interest in pharmaceutical research. Safety data should be consulted for handling and storage, as with all chemical substances, to ensure proper precautions are taken.
Formula:C6H7FN2
InChI:InChI=1/C6H7FN2/c1-4-2-5(8)3-9-6(4)7/h2-3H,8H2,1H3
SMILES:Cc1cc(cnc1F)N
Synonyms:
  • 2-Fluoro-5-Amino-3-Picoline
  • 6-Fluoro-5-Methylpyridin-3-Amine
  • 5-Amino-2-Fluoro-3-Picoline
  • 3-Pyridinamine, 6-fluoro-5-methyl-
  • 5-Amino-2-Fluoro-3-Methylpyridine
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