Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its protected amine group and phenolic hydroxyl functionality allow selective reactions in multi-step organic syntheses. Commonly employed in medicinal chemistry for constructing drug candidates targeting inflammatory and oncological diseases. The bromo substituent enables further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations, making it valuable in structure-activity relationship studies.