Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where bromo-substituted aryl groups facilitate coupling reactions such as Suzuki or Buchwald-Hartwig aminations. The tert-butyl carbamate (Boc) protecting group stabilizes the amine during multi-step syntheses and can be easily removed under mild acidic conditions when needed. Its structure allows for selective functionalization of the aromatic ring, making it valuable in the preparation of drug candidates targeting kinase inhibition and central nervous system disorders. Also employed in agrochemical research for building complex molecules with enhanced stability and specificity.