Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs. Its structure supports the modulation of biological activity in active drug molecules, especially those targeting cyclooxygenase (COX) pathways. The presence of electron-withdrawing nitro and trifluoromethoxy groups enhances binding affinity and metabolic stability. Commonly employed in research settings for designing new nonsteroidal anti-inflammatory drugs (NSAIDs) with improved efficacy and reduced side effects. Also utilized in agrochemical research for developing herbicides due to its ability to influence plant growth regulation through selective enzyme inhibition.