(4-(Piperidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid

(4-(Piperidin-3-yl)-3-(trifluoromethyl)phenyl)boronic acid, with CAS number 2256708-80-0, is a versatile organic compound. It incorporates a boronic acid functional group, which is highly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of new carbon-carbon bonds. The molecule also contains a piperidine ring, a common heterocyclic scaffold in medicinal chemistry, and a trifluoromethyl group, often used to enhance lipophilicity and metabolic stability in drug discovery. This combination of functional groups makes it a useful intermediate for synthesizing complex molecules in pharmaceutical and agrochemical research.

• Handle with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Consult the Safety Data Sheet (SDS) for detailed safety information.