3-Ethenyl-5-fluoropyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a vinyl group (ethenyl) at the 3-position and a fluorine atom at the 5-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid and is known for its reactivity due to the presence of the double bond in the ethenyl group, which can participate in various addition reactions. The fluorine atom enhances the compound's electronegativity, potentially influencing its reactivity and interactions with other chemical species. 3-Ethenyl-5-fluoropyridine is of interest in medicinal chemistry and materials science, where it may serve as a building block for the synthesis of more complex molecules. Its properties, such as solubility and stability, can vary depending on the solvent and environmental conditions. As with many fluorinated compounds, it may exhibit unique biological activities, making it a subject of research in drug development and agrochemicals.

3-Ethenyl-5-fluoropyridine

1133879-69-2: 3-Ethenyl-5-fluoropyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The presence of a vinyl group (ethenyl) at the 3-position and a fluorine atom at the 5-position contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid and is known for its reactivity due to the presence of the double bond in the ethenyl group, which can participate in various addition reactions. The fluorine atom enhances the compound's electronegativity, potentially influencing its reactivity and interactions with other chemical species. 3-Ethenyl-5-fluoropyridine is of interest in medicinal chemistry and materials science, where it may serve as a building block for the synthesis of more complex molecules. Its properties, such as solubility and stability, can vary depending on the solvent and environmental conditions. As with many fluorinated compounds, it may exhibit unique biological activities, making it a subject of research in drug development and agrochemicals.

CAS 1133879-69-2

3-Ethenyl-5-fluoropyridine

Pyridine, 3-ethenyl-5-fluoro-

Ref: IN-DA0008DG

3-Ethenyl-5-fluoropyridine

Ref: 54-PC904618

3-ETHENYL-5-FLUOROPYRIDINE

Ref: 10-F502730