Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting anticancer and antimicrobial agents. The tetrazole moiety serves as a bioisostere for carboxylic acids, improving binding affinity to biological targets. Its structure, featuring a bromo-fluoro phenyl substituent, allows for easy functionalization, making it valuable in medicinal chemistry for developing new drug candidates. Commonly employed in Suzuki and other cross-coupling reactions to build complex aromatic systems. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing properties and stability.