Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds in pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing complex aromatic structures. The presence of electron-withdrawing nitro and trifluoromethyl groups enhances reactivity and influences the electronic properties of the resulting products. Commonly employed in the preparation of intermediates for bioactive molecules, including potential kinase inhibitors and anti-inflammatory agents.