AB48703
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 95% | in stock | $16.00 | $12.00 | - + | |
5g | 95% | in stock | $45.00 | $32.00 | - + | |
10g | 95% | in stock | $78.00 | $55.00 | - + | |
25g | 95% | in stock | $194.00 | $136.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB48703 |
Chemical Name: | 2-Methylpyridine-4-boronic acid pinacol ester |
CAS Number: | 660867-80-1 |
Molecular Formula: | C12H18BNO2 |
Molecular Weight: | 219.0878 |
MDL Number: | MFCD08061590 |
SMILES: | Cc1nccc(c1)B1OC(C(O1)(C)C)(C)C |
Complexity: | 252 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 16 |
Hydrogen Bond Acceptor Count: | 3 |
Rotatable Bond Count: | 1 |
2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis as a key building block. This compound plays a crucial role in various organic reactions due to its unique structural properties and reactivity.One of the primary applications of 2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is as a boron-containing reagent in Suzuki coupling reactions. In these reactions, $name$ serves as a boronic acid source, enabling the formation of carbon-carbon bonds through cross-coupling with aryl or vinyl halides under the catalysis of palladium. This method is widely used in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and materials.Moreover, 2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is also employed in various other transformations, including C-H activation, Buchwald-Hartwig amination, and Heck reactions. Its ability to undergo selective functionalization and regioselective transformations makes it a valuable tool for organic chemists seeking to construct diverse chemical structures efficiently.Overall, the versatile nature of 2-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine makes it a valuable reagent in modern organic synthesis, enabling the rapid and controlled construction of complex molecules with high efficiency and selectivity.