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AB48703

660867-80-1 | 2-Methylpyridine-4-boronic acid pinacol ester

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 -   +

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*All prices are in USD.

Description
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

 

Computed Properties
Complexity: 252  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 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.
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