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CAS 881381-12-0

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2-Formylthiophene-4-boronic acid pinacol ester

Description:
2-Formylthiophene-4-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety and a thiophene ring with a formyl group. This compound typically exhibits a pale yellow to light brown appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. The presence of the boronic acid functionality allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The formyl group contributes to its reactivity, enabling further functionalization. Additionally, the pinacol ester serves as a protective group for the boronic acid, enhancing stability and facilitating handling. This compound is of interest in materials science and medicinal chemistry due to its potential applications in the synthesis of complex organic molecules and pharmaceuticals. As with many organoboron compounds, care should be taken in handling due to potential reactivity and the need for proper storage conditions to maintain stability.
Formula:C11H15BO3S
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