Used as a key building block in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its strained cyclopropane ring and fluorinated substituents make it valuable for introducing fluorinated motifs into target molecules, which is highly relevant in pharmaceutical and agrochemical research. The pinacol ester group enhances stability and handling, making it a practical reagent for late-stage functionalization in drug discovery. Commonly employed to develop bioactive compounds where fluorine atoms improve metabolic stability, lipophilicity, and binding affinity.