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CAS 758699-74-0

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4-Methoxypyridine-3-boronic acid pinacol ester

Description:
4-Methoxypyridine-3-boronic acid pinacol ester is an organoboron compound characterized by the presence of a pyridine ring substituted with a methoxy group and a boronic acid moiety that is esterified with pinacol. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols and other nucleophiles, making it useful in various organic synthesis applications, particularly in Suzuki-Miyaura cross-coupling reactions. The methoxy group enhances the electron density of the pyridine ring, potentially influencing its reactivity and solubility in organic solvents. Additionally, the pinacol ester form stabilizes the boronic acid, allowing for easier handling and storage. This compound is often utilized in the synthesis of complex organic molecules, pharmaceuticals, and agrochemicals due to its versatile reactivity. Its unique structural features contribute to its utility in medicinal chemistry and materials science, where boron-containing compounds play a significant role in drug development and the creation of functional materials.
Synonyms:
  • 4-Methoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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