Used as a coupling reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its stability and reactivity make it suitable for constructing biaryl compounds, which are common structural motifs in drug development. The trifluoroborate group enhances shelf life and reduces toxicity compared to boronic acids, offering a safer and more practical alternative in large-scale applications. It is particularly effective in palladium-catalyzed reactions under mild conditions, allowing for high functional group tolerance.