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-Fluoro-5-vinylpyridine, Pyridine, 3-ethenyl-5-fluoro-, 3-Ethenyl-5-fluoropyridine

3-Ethenyl-5-fluoropyridine is a fluorinated analog of tetrahydrocarbazole that binds to the neuronal nicotinic acetylcholine receptor. It is a radioligand for use in binding studies and has been shown to have a high affinity for the neuronal nAChR. 3-Ethenyl-5-fluoropyridine has been shown to be an effective catalyst for fluoride ion, which may be due to its ability to bind to fluoride ions more tightly than other ligands. This compound also modifies the properties of the enzyme catalysis, which is required for the conversion of glucose into carbon dioxide and water.

CAS 1133879-69-2: 3-Ethenyl-5-fluoropyridine

3-Ethenyl-5-fluoropyridine

Ref: 3D-IVB87969

Pyridine, 3-ethenyl-5-fluoro-

Ref: IN-DA0008DG

3-Ethenyl-5-fluoropyridine

Ref: 54-PC904618

3-ETHENYL-5-FLUOROPYRIDINE

Ref: 10-F502730