This compound, (4-(piperidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid, features a piperidin-3-yl substituent, a trifluoromethyl group, and a boronic acid moiety attached to a phenyl ring. It is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, serving as a key intermediate in the construction of complex molecules. This is especially relevant in pharmaceutical research and development, including the synthesis of biologically active compounds for potential drug candidates targeting neurological disorders or receptor-mediated conditions. The boronic acid group enables efficient coupling with aryl halides to form carbon-carbon bonds, while the trifluoromethyl group enhances lipophilicity and metabolic stability of the resulting molecules, offering advantages in medicinal chemistry. The piperidine moiety contributes to potential interactions with biological receptors. Additionally, the compound is explored in materials science for designing advanced organic materials with specific electronic or optical properties.