Used as a key intermediate in the synthesis of pharmaceutical agents targeting kinase inhibition, particularly in anticancer drug development. Its structure supports binding to enzyme active sites involved in signal transduction pathways, making it valuable in the design of small-molecule inhibitors. Commonly employed in research for developing compounds with activity against tyrosine kinase receptors, which play roles in tumor growth and proliferation. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize potency, selectivity, and pharmacokinetic properties of drug candidates.