Used as a reagent in organic synthesis, particularly in cross-coupling reactions to introduce trifluoroborated aryl groups. It serves as a stable boron-based nucleophile in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates. Its stability and reactivity make it suitable for late-stage functionalization in complex molecule synthesis. The dimethoxy groups enhance solubility and can influence regioselectivity in reactions. Commonly applied in the preparation of bioactive compounds and functional materials requiring fluorinated building blocks.