CAS · 150255-96-2
Product Overview
3-Cyanophenylboronic acid is a high-purity oled-materials supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.
Product Specifications
| Appearance | White solid |
|---|---|
| Purity (HPLC) | 99% min |
| 1H NMR | Consistent to structure |
Applications
3-Cyanophenylboronic acid is an important boronic acid derivative extensively used in organic synthesis, medicinal chemistry, and material sciences. Its primary application is in Suzuki–Miyaura cross-coupling reactions, where it serves as a building block for the formation of biaryl structures, heteroaryl derivatives, and other complex organic molecules. In pharmaceutical research, it is employed as a key intermediate for the synthesis of bioactive compounds, including kinase inhibitors, enzyme modulators, and drug candidates with enhanced pharmacological properties. In materials science, 3-cyanophenylboronic acid is applied in the preparation of functional polymers, electronic materials, and sensors, benefiting from its boronic acid functionality and cyano group reactivity.
Benefits
The benefits of 3-cyanophenylboronic acid arise from its versatile reactivity, stability, and ability to introduce both boronic and nitrile functionalities into target molecules. Its cyano group provides an electron-withdrawing effect, which enhances reaction selectivity and allows for further chemical transformations such as reduction, hydrolysis, or cyclization. Its compatibility with palladium-catalyzed cross-coupling makes it a highly efficient and reliable reagent for constructing C–C bonds in complex molecules. Furthermore, it is stable under typical storage conditions, soluble in common organic solvents, and easily incorporated into large-scale synthesis, ensuring reproducibility and scalability in research and industrial applications.
Conclusion
In summary, 3-cyanophenylboronic acid is a valuable intermediate in organic, pharmaceutical, and material chemistry. Its benefits include dual functional reactivity, high stability, and suitability for efficient cross-coupling reactions. By enabling the construction of advanced molecular architectures with precision, 3-cyanophenylboronic acid plays a crucial role in drug discovery, fine chemical production, and the development of innovative materials.
Previous
4-Bromo-3-chloro-1,1-biphenyl丨CAS 91354-08-4
Next