2,3-Difluoro-6-methylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with two fluorine atoms at the 2 and 3 positions and a methyl group at the 6 position. This compound is part of the pyridine family, which is known for its aromatic properties and basicity due to the nitrogen atom in the ring. The presence of fluorine atoms introduces significant electronegativity, influencing the compound's reactivity and polarity. Typically, such substitutions can enhance the compound's solubility in polar solvents and alter its interaction with biological systems, making it of interest in medicinal chemistry and agrochemical applications. The methyl group contributes to the steric and electronic properties of the molecule, potentially affecting its behavior in chemical reactions. 2,3-Difluoro-6-methylpyridine may also exhibit unique spectral characteristics, making it identifiable through techniques such as NMR and mass spectrometry. Overall, its specific structure allows for diverse applications in research and industry, particularly in the development of pharmaceuticals and specialty chemicals.

2,3-difluoro-6-methylpyridine

1227579-04-5: 2,3-Difluoro-6-methylpyridine is a heterocyclic organic compound characterized by a pyridine ring substituted with two fluorine atoms at the 2 and 3 positions and a methyl group at the 6 position. This compound is part of the pyridine family, which is known for its aromatic properties and basicity due to the nitrogen atom in the ring. The presence of fluorine atoms introduces significant electronegativity, influencing the compound's reactivity and polarity. Typically, such substitutions can enhance the compound's solubility in polar solvents and alter its interaction with biological systems, making it of interest in medicinal chemistry and agrochemical applications. The methyl group contributes to the steric and electronic properties of the molecule, potentially affecting its behavior in chemical reactions. 2,3-Difluoro-6-methylpyridine may also exhibit unique spectral characteristics, making it identifiable through techniques such as NMR and mass spectrometry. Overall, its specific structure allows for diverse applications in research and industry, particularly in the development of pharmaceuticals and specialty chemicals.

CAS 1227579-04-5

2,3-difluoro-6-methylpyridine

2,3-Difluoro-6-methylpyridine

Ref: 54-PC906336

2,3-Difluoro-6-methyl-pyridine

Ref: 10-F386285