Widely used in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to introduce trifluoromethyl-substituted aromatic systems into complex molecules. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in pharmaceutical and agrochemical synthesis. The presence of the electron-withdrawing trifluoromethyl group enhances reactivity and influences the pharmacokinetic properties of target compounds. Commonly employed in the preparation of bioactive molecules, including drug candidates where trifluoromethyl motifs improve metabolic stability and membrane permeability. Also utilized in materials science for constructing functional organic materials with tailored electronic properties.