Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex fluorinated organic molecules for pharmaceuticals and agrochemicals. The boronate ester group facilitates efficient carbon-carbon bond formation under mild conditions. Its naphthalene backbone with fluoro and methoxymethoxy substituents enhances electronic and steric properties, making it valuable in developing bioactive compounds and functional materials. Commonly employed in medicinal chemistry for constructing fluorinated drug candidates with improved metabolic stability and binding affinity.