Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting enzymes involved in inflammatory and oncological pathways. Shows potential in modulating cellular signaling due to its structural affinity for ATP-binding sites in protein kinases. Also employed in the development of selective modulators of central nervous system receptors, with studies exploring its role in neurodegenerative and psychiatric disorder treatments. Its fluorinated aryl group enhances metabolic stability and bioavailability, making it valuable in optimizing drug candidates for in vivo efficacy.