(2-Fluoro-6-(methylamino)pyridin-3-yl)boronic acid
≥95%
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable for constructing complex molecules in pharmaceutical and material science research. It is often employed in the development of drug candidates, where its pyridine and fluorine components can enhance binding affinity and metabolic stability. Additionally, it serves as a building block for creating advanced materials, such as organic semiconductors or catalysts, due to its ability to introduce specific functional groups into target structures. Its applications are largely focused on precision chemistry in research and industrial settings.
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