Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of indole-based drug candidates. Its boronic acid functionality enables Suzuki-Miyaura cross-coupling reactions, allowing the formation of carbon-carbon bonds essential for constructing complex molecular architectures. The presence of both Boc-protected amine and methyl ester groups provides orthogonal reactivity, making it valuable in multi-step syntheses where selective transformations are required. Commonly employed in the development of bioactive molecules, including kinase inhibitors and anti-inflammatory agents.