4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is an organic compound characterized by its pyridine ring substituted with a fluorine atom and a boron-containing moiety. The presence of the fluorine atom enhances its reactivity and can influence its electronic properties, making it useful in various chemical applications. The boron-containing group, specifically the tetramethyl-1,3,2-dioxaborolane, is known for its ability to participate in cross-coupling reactions, which are pivotal in organic synthesis, particularly in the formation of carbon-carbon bonds. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its unique structure suggests potential applications in medicinal chemistry, agrochemicals, or materials science, where the combination of fluorine and boron can impart desirable properties such as increased stability or enhanced biological activity. As with many boron-containing compounds, it may also exhibit interesting coordination chemistry, making it a candidate for further research in coordination complexes or catalysis.

4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

1220219-91-9: 4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is an organic compound characterized by its pyridine ring substituted with a fluorine atom and a boron-containing moiety. The presence of the fluorine atom enhances its reactivity and can influence its electronic properties, making it useful in various chemical applications. The boron-containing group, specifically the tetramethyl-1,3,2-dioxaborolane, is known for its ability to participate in cross-coupling reactions, which are pivotal in organic synthesis, particularly in the formation of carbon-carbon bonds. This compound is likely to be a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its unique structure suggests potential applications in medicinal chemistry, agrochemicals, or materials science, where the combination of fluorine and boron can impart desirable properties such as increased stability or enhanced biological activity. As with many boron-containing compounds, it may also exhibit interesting coordination chemistry, making it a candidate for further research in coordination complexes or catalysis.

4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

4-Fluoropyridine-3-boronic acid pinacol ester

CAS 1220219-91-9

4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Ref: IN-DA0016MZ

4-Fluoropyridine-3-boronic acid pinacol ester

Ref: 54-PC510169