Used as a reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, specifically aryl-benzyl linkages, in organic synthesis. Its stability and reactivity make it suitable for constructing diarylmethane compounds (Ar-CH₂-Ar), which are common structural motifs in pharmaceuticals and agrochemicals. The presence of the trifluoroborate group enhances handling and shelf life compared to boronic acids, while the 2-chlorobenzyl moiety allows for further functionalization or participation in selective coupling processes. Commonly applied in medicinal chemistry for the development of drug candidates requiring aryl-alkyl linkages.