Used as a key intermediate in the synthesis of selective kinase inhibitors, particularly in the development of anticancer agents. Its structure enables strong binding to specific enzyme targets involved in cell signaling pathways, making it valuable in pharmaceutical research for targeted therapies. It has shown potential in inhibiting tyrosine kinases associated with tumor growth and inflammation. Due to its fluorinated and chlorinated aromatic systems, it enhances metabolic stability and bioavailability in drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize potency and selectivity.