Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly those targeting cyclin-dependent kinases (CDKs) involved in cancer cell proliferation. Shows potential in developing antitumor agents due to its ability to enhance binding affinity and selectivity in inhibitor design. Also explored for antiviral applications owing to structural similarity with known viral replication inhibitors. Its fluorinated aromatic ring improves metabolic stability and membrane permeability, making it suitable for drug development. Investigated in the design of anti-inflammatory compounds by modulating signaling pathways linked to cytokine production.