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181219-01-2

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

Catalog#: AR003MPG  |   CAS#: 181219-01-2  |   MDL#: MFCD01319051  |   MF: C11H16BNO2  |   MW: 205.0612

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1g 97% $3.00 Global Stock Buy Now Add To Cart
5g 97% $7.00 Global Stock Buy Now Add To Cart
10g 97% $11.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003MPG
Chemical Name 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS Number 181219-01-2
Molecular Formula C11H16BNO2
Molecular Weight 205.0612
MDL Number MFCD01319051
SMILES CC1(C)OB(OC1(C)C)c1ccncc1

The 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile reagent commonly used in chemical synthesis. This compound serves as a valuable building block in various organic reactions due to its unique properties.One key application of 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is its ability to act as a ligand in transition metal-catalyzed cross-coupling reactions. When combined with palladium or nickel catalysts, this compound facilitates the formation of carbon-carbon and carbon-heteroatom bonds, allowing for the efficient construction of complex molecular structures.Additionally, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine can be utilized in Suzuki-Miyaura reactions, a widely employed method for the synthesis of biaryls. By serving as a boron source in these coupling reactions, this compound enables the selective formation of aryl-aryl linkages, offering a powerful tool for the preparation of pharmaceuticals, agrochemicals, and materials.Overall, the use of 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine in chemical synthesis contributes to the efficient and selective construction of organic molecules, highlighting its significance in modern synthetic chemistry.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302+H312+H332-H315-H319-H335
Precautionary Statements P261-P280-P305+P351+P338
Class N/A
Packing Group N/A

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