Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of receptor modulators and central nervous system agents. Its structure supports the construction of sterically hindered amines, which are common in drug candidates targeting neurological disorders. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other sites during multi-step synthesis. The bromophenyl moiety enables further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in medicinal chemistry for generating compound libraries.