(2-Cyclopropyl-5-(trifluoromethyl)pyridin-3-yl)boronic acid

(2-Cyclopropyl-5-(trifluoromethyl)pyridin-3-yl)boronic acid, identified by CAS 2225176-76-9, is a sophisticated pyridine derivative. This compound features a boronic acid moiety, a cyclopropyl ring, and a trifluoromethyl group, making it a highly versatile and reactive intermediate for advanced organic synthesis. Its boronic acid functionality is particularly useful for forming new carbon-carbon bonds through cross-coupling reactions, such as the Suzuki-Miyaura coupling. The trifluoromethyl group can introduce specific electronic and steric properties, often beneficial for enhancing metabolic stability or lipophilicity in synthesized target molecules. The cyclopropyl group contributes to structural rigidity and can influence molecular conformation. This chemical is intended for research applications requiring complex synthetic building blocks.

• Handle with appropriate personal protective equipment (PPE), including chemical-resistant gloves, eye protection, and a lab coat. Use in a well-ventilated area or a fume hood to prevent inhalation. Avoid direct contact with skin and eyes. In case of exposure, rinse affected areas immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Always consult the Safety Data Sheet (SDS) for comprehensive hazard information and detailed safe handling procedures. This product is for Research Use Only (RUO).