2-Chloro-5-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
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This compound is primarily utilized in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of both chloro and fluoro substituents on the pyridine ring enhances its reactivity and selectivity, allowing for precise modifications in drug discovery and material science applications. Additionally, it serves as an intermediate in the development of bioactive compounds, where its structural features contribute to the fine-tuning of molecular properties.
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