Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The presence of a cyclohexylcarbamoyl moiety enhances solubility and stability, making it suitable for solid-phase synthesis and medicinal chemistry applications. Commonly employed in the development of protease inhibitors and kinase modulators due to its ability to mimic peptide bonds and interact with biological targets. Also utilized in sensor design for detecting diols and saccharides owing to the reversible esterification capability of the boronic acid functional group.