Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its furan-containing structure makes it valuable for constructing conjugated systems in pharmaceuticals, agrochemicals, and organic electronic materials. The borolane group provides high stability and reactivity under palladium catalysis, allowing efficient coupling with aryl or heteroaryl halides. It exhibits good stability towards air and water compared to other boronates, facilitating easier storage and handling. Additionally, the attached tetrahydrofuran group enhances solubility in organic solvents. Commonly employed in late-stage functionalization due to its compatibility with various functional groups.