Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, enhancing antimicrobial activity against a broad spectrum of bacteria. Its structure supports the development of drugs targeting DNA gyrase and topoisomerase IV, critical for bacterial replication. Also explored in medicinal chemistry for antimalarial and anticancer agents due to its ability to chelate metal ions and interact with biological targets. Employed in research for developing new fluorinated heterocyclic compounds with improved pharmacokinetic properties.