Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its halogenated pyridine structure makes it valuable in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig aminations, enabling the construction of complex heterocyclic systems. The presence of both bromine and trifluoromethoxy groups allows for selective functionalization, facilitating the optimization of pharmacokinetic properties in drug discovery programs. Commonly employed in research settings for designing kinase inhibitors and receptor modulators.