The compound features a boronic acid functionality (-B(OF)2) attached to a phenyl ring, and it is further substituted with fluorine atoms at the 2- and 3-positions. This specific arrangement defines its chemical structure.The boronic acid group makes the compound a valuable building block in organic synthesis, especially in Suzuki-Miyaura cross-coupling reactions. The fluorine substituents contribute to the compound's reactivity and electronic properties.
features：
The boronic acid group makes the compound a versatile building block in organic synthesis. Boronic acids are known for their ability to form stable complexes with diols, and they are widely used in Suzuki-Miyaura cross-coupling reactions for carbon-carbon bond formation.
Applications:
One of the main applications of 2,3-difluorophenylboronic acid is the Suzuki-Miyaura cross-coupling reaction. It is a key reagent in the formation of carbon-carbon bonds, allowing the introduction of boric acid functional groups into various organic molecules. This is especially important in the synthesis of pharmaceutical, agricultural, and other fine chemicals.
