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CAS 179898-50-1

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3-CHLORO-2-METHOXYPHENYLBORONIC ACID

Description:
3-Chloro-2-methoxyphenylboronic 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 chemical reactions, particularly in Suzuki coupling reactions. This compound features a chloro substituent and a methoxy group on a phenyl ring, which can influence its reactivity and solubility. The presence of the boronic acid group allows for participation in cross-coupling reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its molecular structure contributes to its potential applications in medicinal chemistry, particularly in the development of targeted therapies. Additionally, the compound's properties, such as solubility in organic solvents and stability under certain conditions, are essential for its practical use in laboratory and industrial settings. Overall, 3-chloro-2-methoxyphenylboronic acid is a versatile reagent in organic synthesis with significant implications in various fields of chemistry.
Formula:C7H8BClO3
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