AD70352
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 96% | in stock | $33.00 | $23.00 | - + | |
1g | 96% | in stock | $43.00 | $30.00 | - + | |
5g | 96% | in stock | $136.00 | $95.00 | - + | |
10g | 96% | in stock | $267.00 | $187.00 | - + | |
25g | 96% | in stock | $511.00 | $358.00 | - + | |
100g | 96% | in stock | $1,319.00 | $923.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AD70352 |
Chemical Name: | 3-Bromo-2-cyanophenylboronic acid |
CAS Number: | 1032231-32-5 |
Molecular Formula: | C7H5BBrNO2 |
Molecular Weight: | 225.8351 |
MDL Number: | MFCD10696672 |
SMILES: | N#Cc1c(Br)cccc1B(O)O |
Complexity: | 203 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 1 |
(3-Bromo-2-cyanophenyl)boronic acid is a highly versatile compound commonly used in organic synthesis. It serves as a key building block in the preparation of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties.In chemical synthesis, (3-Bromo-2-cyanophenyl)boronic acid acts as a critical reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the formation of carbon-carbon bonds, allowing for the creation of complex organic molecules. By participating in this coupling reaction, (3-Bromo-2-cyanophenyl)boronic acid enables the selective and efficient assembly of organic compounds with precision.Additionally, (3-Bromo-2-cyanophenyl)boronic acid can also be utilized in transition metal-catalyzed cross-coupling reactions to facilitate the construction of biaryls, heteroaromatics, and other challenging chemical structures. Its ability to undergo diverse chemical transformations makes it a valuable tool for synthetic chemists seeking to develop novel compounds with specific properties.Overall, the application of (3-Bromo-2-cyanophenyl)boronic acid in chemical synthesis plays a crucial role in expanding the synthetic toolbox available to researchers, enabling the efficient and controlled construction of complex organic molecules for various applications.