Used in pharmaceutical research as a key intermediate in the synthesis of selective kinase inhibitors, particularly those targeting inflammatory and oncological pathways. Its structural configuration supports high binding affinity to specific enzyme active sites, making it valuable in developing drugs for autoimmune diseases and certain cancers. The compound's fluorinated aromatic system and chiral piperidine core enhance metabolic stability and target selectivity. It is also employed in structure-activity relationship (SAR) studies to optimize potency and pharmacokinetic properties in drug candidates.