Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boron-containing structure acts as a coupling partner with aryl or vinyl halides in the presence of a palladium catalyst, facilitating the introduction of the 2,3,6-trifluorophenyl group into complex molecules. This makes it valuable in the development of fluorinated organic compounds, which often exhibit enhanced metabolic stability and bioavailability. Commonly employed in late-stage functionalization during drug discovery and in the preparation of advanced intermediates for materials science applications.