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CAS 1112208-82-8

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2-Fluoro-5-formylphenylboronic acid pinacol ester

Description:
2-Fluoro-5-formylphenylboronic acid pinacol ester is a chemical compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications. The compound features a fluorine atom at the 2-position and a formyl group at the 5-position of a phenyl ring, contributing to its reactivity and potential applications in medicinal chemistry and material science. The pinacol ester moiety enhances the stability of the boronic acid, allowing for easier handling and storage. This compound is typically used in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Its unique structural characteristics enable it to participate in diverse chemical transformations, making it a valuable intermediate in the synthesis of complex organic molecules. As with many boronic acids and their derivatives, care should be taken in handling due to potential reactivity and the need for specific storage conditions to maintain stability.
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