Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical and agrochemical research. The iodine substituent allows for further functionalization via cross-coupling reactions such as Suzuki or Heck couplings, enabling the construction of complex pyrazole derivatives. The tert-butoxycarbonyl (Boc) group protects the pyrazole nitrogen during synthetic transformations and can be easily removed under mild acidic conditions when needed. This compound is especially valuable in medicinal chemistry for developing kinase inhibitors, anti-inflammatory agents, and other drug candidates where the pyrazole core is a structural motif.