(4-Chlorophenyl)boronic acid(CAS: 1679-18-1)

(4-Chlorophenyl)boronic acid, with the CAS number 1679-18-1, is an organic compound that contains a boronic acid group attached to a 4-chlorophenyl ring. It is a white crystalline solid with a molecular formula of C7H7ClBO2 and is known for its reactivity in various chemical reactions, particularly in Suzuki coupling and other transition metal-catalyzed processes. This compound is commonly used in synthetic chemistry due to its functional group versatility.

(4-Chlorophenyl)boronic acid (CAS: 1679-18-1) is primarily used in pharmaceutical research for the synthesis of various drugs and bioactive compounds. It also finds applications in industrial chemical processes, particularly in the development of materials and intermediates. In research settings, it serves as a key reagent in organic synthesis and catalytic reactions, making it valuable for creating complex molecules with specific functionalities.

While (4-Chlorophenyl)boronic acid (CAS: 1679-18-1) is generally considered safe when handled properly, it should be treated with caution. It is advisable to use appropriate personal protective equipment (PPE) such as gloves and goggles to avoid skin contact or inhalation. Although it is not classified as highly toxic, it is important to follow standard safety protocols and storage guidelines to ensure safe handling in laboratories and industrial environments.

(4-Chlorophenyl)boronic acid (CAS: 1679-18-1) should be stored in a cool, dry, and well-ventilated area away from direct light. It is recommended to keep it in a sealed container to prevent moisture absorption and maintain stability. Proper storage conditions include temperatures below 25°C and low humidity levels to avoid degradation and ensure long-term usability.