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 allows for efficient and selective coupling with aryl halides under mild conditions. Particularly valuable in late-stage functionalization of complex molecules due to its stability and reactivity profile. Commonly employed in the development of fluorinated organic compounds where the trifluoromethoxy group influences metabolic stability and lipophilicity.