(2-Chloro-6-fluoro-3-hydroxy-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. This compound features a phenyl ring substituted with a chlorine atom at the 2-position, a fluorine atom at the 6-position, and a hydroxyl group at the 3-position, contributing to its unique reactivity and potential applications in medicinal chemistry and organic synthesis. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the halogen substituents can influence the electronic properties of the compound, affecting its reactivity and interactions with biological targets. Its solubility and stability in various solvents can vary, which is important for its application in laboratory settings. Overall, this compound is of interest in the development of pharmaceuticals and materials science due to its versatile chemical properties.

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

957121-07-2: (2-Chloro-6-fluoro-3-hydroxyphenyl)boronic acid, boronic acid, B-(2-chloro-6-fluoro-3-hydroxyphenyl)-, 2-Chloro-6-Fluoro-3-Hydroxyphenylboronic Acid

2-Chloro-6-fluoro-3-hydroxyphenylboronic acid

2-Chloro-6-fluoro-3-hydroxybenzeneboronic acid

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CAS 957121-07-2: (2-chloro-6-fluoro-3-hydroxy-phenyl)boronic acid

2-Chloro-6-fluoro-3-hydroxyphenylboronic acid

Ref: IN-DA006BL3

2-Chloro-6-fluoro-3-hydroxyphenylboronic acid

Ref: 10-F225341

2-Chloro-6-fluoro-3-hydroxybenzeneboronic acid

Ref: 54-PC8335

(2-Chloro-6-fluoro-3-hydroxyphenyl)boronic acid

Ref: 3D-FC90794