Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting agents targeting neurological pathways. Its structure supports the creation of bioactive molecules due to the stability imparted by the tert-butyl carbamate group and the conformational restraint of the cyclopropane ring. Commonly employed in medicinal chemistry for constructing analogs in structure-activity relationship (SAR) studies, especially in programs focused on receptor modulators. The bromine substituent allows further functionalization via cross-coupling reactions such as Suzuki or Heck reactions, enabling rapid diversification for drug discovery.