(6-Chloro-2-fluoro-3-methoxy-phenyl)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, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a chlorine atom at the 6-position, a fluorine atom at the 2-position, and a methoxy group at the 3-position, contributing to its unique reactivity and solubility properties. The presence of these halogen and methoxy substituents can influence the electronic properties of the molecule, potentially enhancing its reactivity in cross-coupling reactions, such as Suzuki-Miyaura coupling. Additionally, boronic acids are often utilized in the development of pharmaceuticals and agrochemicals due to their ability to participate in diverse chemical transformations. The compound's specific characteristics, such as melting point, solubility, and stability, would typically be determined through experimental methods and may vary based on the conditions of use.

(6-chloro-2-fluoro-3-methoxy-phenyl)boronic acid

867333-04-8: 6-Chloro-2-Fluoro-3-Methoxyphenylboronicacid

6-Chloro-2-fluoro-3-methoxyphenylboronicacid

6-Chloro-2-fluoro-3-methoxyphenylboronic acid

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CAS 867333-04-8: (6-chloro-2-fluoro-3-methoxy-phenyl)boronic acid

6-Chloro-2-fluoro-3-methoxyphenylboronicacid

Ref: IN-DA008F7Z

6-Chloro-2-fluoro-3-methoxyphenylboronic acid

Ref: 54-PC412090

6-Chloro-2-fluoro-3-methoxyphenylboronic acid

Ref: 10-F044127

(6-chloro-2-fluoro-3-methoxy-phenyl)boronic acid

Ref: 3D-FC91202