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CAS 957121-15-2

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6-Bromo-2-chloro-3-ethoxyphenylboronic acid

Description:
6-Bromo-2-chloro-3-ethoxyphenylboronic 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. The compound features a phenyl ring substituted with both a bromine and a chlorine atom, contributing to its reactivity and potential applications in medicinal chemistry and material science. The ethoxy group enhances its solubility in organic solvents, facilitating its use in synthetic processes. Additionally, the presence of halogen substituents can influence the electronic properties of the molecule, affecting its reactivity and interaction with biological targets. As a boronic acid, it can also participate in the formation of boronate esters, which are important in the development of drug delivery systems and in the synthesis of complex organic molecules. Overall, 6-Bromo-2-chloro-3-ethoxyphenylboronic acid is a versatile compound with significant implications in organic synthesis and pharmaceutical research.
Formula:C8H9BBrClO3
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