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CAS 909122-50-5

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3-chloro-4-ethoxy-2-fluorophenylboronic acid

Description:
3-Chloro-4-ethoxy-2-fluorophenylboronic 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 phenyl ring substituted with a chlorine atom at the 3-position, an ethoxy group at the 4-position, and a fluorine atom at the 2-position, contributing to its unique reactivity and solubility properties. The boronic acid moiety enhances its utility in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the presence of halogen substituents can influence the electronic properties of the molecule, potentially affecting its biological activity and interaction with other chemical species. Overall, 3-chloro-4-ethoxy-2-fluorophenylboronic acid is a versatile compound with significant implications in synthetic organic chemistry and pharmaceutical development.
Formula:C8H9BClFO3
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