(3-Chloro-5-methylphenyl)boronic acid(CAS: 913836-14-3)

(3-Chloro-5-methylphenyl)boronic acid is a chemical compound with the CAS number 913836-14-3. It is an organic boronic acid derivative characterized by its aromatic ring structure, featuring a chloro and methyl substituent. This compound is commonly used in organic synthesis and as a reagent in various chemical reactions.

(3-Chloro-5-methylphenyl)boronic acid is widely used in pharmaceutical and chemical industries, particularly in organic synthesis. It serves as a key reagent in Suzuki coupling reactions and other palladium-catalyzed cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules.

(3-Chloro-5-methylphenyl)boronic acid (CAS: 913836-14-3) is generally considered safe when used and stored correctly. However, it should be handled with caution due to its chemical nature. Protective measures include wearing gloves, goggles, and a lab coat. Exposure to light and moisture should be minimized, and it should be stored in a dry, well-ventilated area away from direct sunlight and heat sources.

(3-Chloro-5-methylphenyl)boronic acid should be stored in a tightly closed container in a cool, dry place away from direct sunlight and sources of heat. The storage temperature should be maintained below 25°C, and the container should be protected from moisture to prevent degradation of the compound. Adequate ventilation is recommended to avoid the accumulation of potentially flammable gases during storage.