4-Cvanophenylboronic acid CAS: 126747-14-6
Catalog Number | XD94126 |
Product Name | 4-Cvanophenylboronic acid |
CAS | 126747-14-6 |
Molecular Formula | C7H6BNO2 |
Molecular Weight | 146.94 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
4-Cyanophenylboronic acid is a versatile chemical compound that finds extensive applications in various fields, including organic synthesis, medicinal chemistry, and materials science. With its unique structural and chemical properties, this compound serves as a valuable building block for the development of diverse molecules and materials.
One of the primary uses of 4-cyanophenylboronic acid is in organic synthesis. It acts as a key reagent for the formation of carbon-carbon bonds through cross-coupling reactions, specifically Suzuki-Miyaura coupling. This powerful synthetic method allows for the efficient and selective construction of complex organic molecules. By combining 4-cyanophenylboronic acid with appropriate coupling partners, chemists can create a wide range of functionalized compounds, including pharmaceutical intermediates, agrochemicals, and fine chemicals.
In medicinal chemistry, 4-cyanophenylboronic acid plays a crucial role in the development of pharmaceuticals. It can be incorporated into drug molecules as a pharmacophore, imparting desirable properties such as improved solubility, stability, and target specificity. Furthermore, this compound can act as a molecular probe in the study of biological systems, aiding in the identification and characterization of specific protein targets.
Moreover, 4-cyanophenylboronic acid is utilized in materials science for the synthesis of functional materials. Its boronic acid functionality enables it to act as a building block for the creation of polymer structures via polymerization reactions. These polymers exhibit unique properties such as stimuli-responsive behavior, self-assembly, and biocompatibility. Such materials find applications in areas such as drug delivery systems, sensors, and electronic devices.
The versatility of 4-cyanophenylboronic acid extends beyond its direct applications. It can also serve as a precursor for the synthesis of other boronic acid derivatives, expanding the range of available compounds. These derivatives can possess different substituents or functional groups, allowing for further customization and tailoring of their properties.
In summary, 4-cyanophenylboronic acid is a valuable compound with diverse applications in organic synthesis, medicinal chemistry, and materials science. Its ability to form carbon-carbon bonds, act as a pharmacophore, and serve as a building block for functional materials makes it an indispensable tool for scientists and researchers in various fields.