3-Borono-2-fluorobenzoic acid is an organic compound characterized by the presence of a boron functional group and a fluorine atom attached to a benzoic acid structure. This compound features a boronic acid moiety, 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 fluorine atom introduces unique electronic properties, enhancing the compound's reactivity and potential interactions in biological systems. Typically, 3-Borono-2-fluorobenzoic acid is a solid at room temperature and is soluble in polar solvents, which facilitates its use in chemical reactions. Its structure allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the compound may exhibit specific biological activities, making it a candidate for further research in drug development and material science. Overall, its unique functional groups contribute to its versatility in synthetic chemistry and potential applications in pharmaceuticals.

3-Borono-2-fluorobenzoic acid

1072952-09-0: Benzoic acid, 3-borono-2-fluoro-, 3-Carboxy-2-fluorophenylboronic acid, 3-Borono-2-fluorobenzoic acid

3-Carboxy-2-fluorophenylboronic acid

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CAS 1072952-09-0: 3-Borono-2-fluorobenzoic acid

3-Carboxy-2-fluorophenylboronic acid

Ref: FT-C10240

3-Borono-2-fluorobenzoic acid

Ref: IN-DA007ERX

3-Carboxy-2-fluorophenylboronic acid

Ref: 54-PC412048

3-Borono-2-fluorobenzoic acid

Ref: 10-F218896

3-borono-2-fluorobenzoic Acid

Ref: 3D-FB105085