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CAS 1119899-50-1

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(5-cyano-4-methylthiophen-2-yl)boronic acid

Description:
(5-Cyano-4-methylthiophen-2-yl)boronic acid is an organoboron 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 applications, including organic synthesis and medicinal chemistry. The compound features a thiophene ring, which contributes to its aromatic properties and potential electronic interactions. The cyano group (-CN) enhances the compound's reactivity and polarity, while the methylthio group (-S-CH3) can influence its solubility and stability. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its boronic acid functionality allows it to participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is valuable in the synthesis of complex organic molecules. Overall, (5-cyano-4-methylthiophen-2-yl)boronic acid is a versatile building block in organic chemistry, particularly in the development of pharmaceuticals and agrochemicals.
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