Used in the synthesis of pharmaceuticals and agrochemicals due to its reactivity as an isocyanate. The electron-withdrawing trifluoromethoxy group enhances stability and influences the electronic properties of final compounds. Commonly employed in the preparation of ureas and urethanes through reactions with amines or alcohols. Valuable intermediate in the development of bioactive molecules, including herbicides and fungicides, where the trifluoromethoxy moiety contributes to improved metabolic stability and membrane permeability. Also utilized in materials science for designing specialty polymers with enhanced thermal and chemical resistance.