2,2-Difluoro-1-(2-pyridyl)ethanone is an organic compound characterized by the presence of a pyridine ring and a ketone functional group. It features two fluorine atoms attached to the carbon adjacent to the carbonyl group, which significantly influences its chemical reactivity and physical properties. The compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. Its molecular structure contributes to its polar nature, which can enhance solubility in polar solvents. The presence of the pyridine moiety may impart biological activity, making it of interest in pharmaceutical research. Additionally, the fluorine substituents can enhance lipophilicity and metabolic stability. The compound is likely to undergo typical reactions associated with ketones, such as nucleophilic addition and condensation reactions. Safety data should be consulted for handling, as fluorinated compounds can exhibit unique toxicity profiles. Overall, 2,2-difluoro-1-(2-pyridyl)ethanone is a versatile compound with potential applications in various fields, including medicinal chemistry and materials science.

2,2-difluoro-1-(2-pyridyl)ethanone

80459-00-3: 2,2-Difluoro-1-(2-pyridyl)ethanone is an organic compound characterized by the presence of a pyridine ring and a ketone functional group. It features two fluorine atoms attached to the carbon adjacent to the carbonyl group, which significantly influences its chemical reactivity and physical properties. The compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. Its molecular structure contributes to its polar nature, which can enhance solubility in polar solvents. The presence of the pyridine moiety may impart biological activity, making it of interest in pharmaceutical research. Additionally, the fluorine substituents can enhance lipophilicity and metabolic stability. The compound is likely to undergo typical reactions associated with ketones, such as nucleophilic addition and condensation reactions. Safety data should be consulted for handling, as fluorinated compounds can exhibit unique toxicity profiles. Overall, 2,2-difluoro-1-(2-pyridyl)ethanone is a versatile compound with potential applications in various fields, including medicinal chemistry and materials science.

CAS 80459-00-3

2,2-difluoro-1-(2-pyridyl)ethanone

2,2-Difluoro-1-(pyridin-2-yl)ethanone

Ref: IN-DA00531C

2-(Difluoroacetyl)pyridine

Ref: 54-PC3462

2,2-Difluoro-1-(pyridin-2-yl)ethanone

Ref: 10-F230285