Get Your 117098-94-9 | 6-aminobenzo[c][1,2]oxaborol-1(3h)-ol - Hot Selling [GkzUi95q]

6-Aminobenzo[c][1,2]oxaborol-1(3H)-ol: A Powerful Boronic Acid Derivative

Introducing the innovative 6-Aminobenzo[c][1,2]oxaborol-1(3H)-ol, a highly effective boronic acid derivative that is a must-have for any researcher or scientist. This product is characterized by its exceptional purity and stability, making it ideal for various applications in the fields of organic synthesis and medicinal chemistry. Its molecular formula, C₇H₈BN₂O₂, and molecular weight of 148.96 g/mol, along with its CAS RN 117098-94-9 and MDL Number MFCD14584713, ensure its traceability and authenticity. The yellow solid appearance of the product signifies its ready-to-use form, offering convenience and efficiency in your research processes.

• High purity: The product meets stringent purity standards, ensuring reliable and reproducible results.
• Stability: The compound is stable, which is crucial for long-term storage and use.

Key Properties and Specifications

This high-quality boronic acid derivative boasts a melting point of 145-148 °C, which is an important parameter for its synthesis and purification processes. Its solid physical state and yellow color are typical of the compound, making it easily identifiable. Although the product's boiling point, density, specific gravity, refractive index, and solubility are not provided, it is advisable to perform further analysis and characterization as per your specific requirements. Storage of this compound is straightforward; simply keep it sealed in a dry environment at room temperature (20 to 22 °C) to maintain its integrity.

• Melting point: 145-148 °C (lit.)
• Storage: Sealed in dry conditions, store at room temperature (20 to 22 °C)

Applications and Benefits

6-Aminobenzo[c][1,2]oxaborol-1(3H)-ol finds a wide range of applications in both research and industrial settings. Its versatility as a boronic acid derivative makes it suitable for various organic transformations, including C-O bond formation and Suzuki coupling reactions. As a target for medicinal chemistry, this compound can be modified to create new pharmaceuticals or lead compounds. Ideal for researchers, scientists, and pharmaceutical companies, this product offers a competitive edge in drug discovery and development. With its strong bond-forming properties and high purity, 6-Aminobenzo[c][1,2]oxaborol-1(3H)-ol is an indispensable tool in the modern laboratory.

• Organic synthesis: Useful in various organic transformations and reactions.
• Medicinal chemistry: Potential for creating new pharmaceuticals and lead compounds.