AA53910
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $209.00 | $147.00 | - + | |
250mg | 95% | in stock | $401.00 | $281.00 | - + | |
1g | 95% | in stock | $867.00 | $607.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA53910 |
Chemical Name: | 5-Formylpyridine-2-boronic acid, hydrate |
CAS Number: | 1217500-70-3 |
Molecular Formula: | C6H8BNO4 |
Molecular Weight: | 168.943 |
MDL Number: | MFCD08703261 |
SMILES: | OC(c1ccc(nc1)B(O)O)O |
Complexity: | 142 |
Covalently-Bonded Unit Count: | 2 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 5 |
Hydrogen Bond Donor Count: | 3 |
Rotatable Bond Count: | 2 |
(5-Formylpyridin-2-yl)boronic acid hydrate is a versatile chemical reagent widely used in chemical synthesis due to its unique properties and functions. As a boronic acid derivative, it plays a crucial role in Suzuki-Miyaura cross-coupling reactions, which are fundamental in the field of organic chemistry for forming carbon-carbon bonds. One key application of (5-Formylpyridin-2-yl)boronic acid hydrate is in the synthesis of biologically active compounds, pharmaceuticals, and functional materials. Its ability to efficiently undergo cross-coupling reactions with various aryl halides or triflates enables the construction of complex molecular structures with high efficiency and selectivity.In addition, (5-Formylpyridin-2-yl)boronic acid hydrate can also be utilized in the preparation of ligands for transition metal-catalyzed reactions, such as palladium-catalyzed C-C and C-N bond formations. This compound serves as a valuable building block in the design and synthesis of novel organic molecules with diverse applications in drug discovery, materials science, and agrochemicals.Overall, the application of (5-Formylpyridin-2-yl)boronic acid hydrate in chemical synthesis offers a powerful tool for organic chemists to access a wide range of structurally complex and biologically important compounds through efficient cross-coupling reactions and functional group transformations.