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741709-62-6

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

Catalog#: AR0033Z3  |   CAS#: 741709-62-6  |   MDL#: MFCD09607734  |   MF: C12H15BN2O2  |   MW: 230.0707

Packsize Purity Price Availability Quantity
100mg 97% $14.00 Global Stock Buy Now Add To Cart
250mg 97% $30.00 Global Stock Buy Now Add To Cart
1g 97% $84.00 Global Stock Buy Now Add To Cart
5g 97% $346.00 Global Stock Buy Now Add To Cart
25g 97% $1,455.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0033Z3
Chemical Name 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinecarbonitrile
CAS Number 741709-62-6
Molecular Formula C12H15BN2O2
Molecular Weight 230.0707
MDL Number MFCD09607734
SMILES N#Cc1nccc(c1)B1OC(C(O1)(C)C)(C)C

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinecarbonitrile, also known as $name$, is a versatile chemical compound widely utilized in chemical synthesis processes. This compound serves as a valuable building block in the creation of various organic molecules due to its unique chemical properties.One of the key applications of $name$ in chemical synthesis is as a boron-containing reagent in Suzuki-Miyaura cross-coupling reactions. This reaction, catalyzed by palladium, enables the formation of carbon-carbon bonds, facilitating the synthesis of complex organic compounds. $name$ acts as a boronic acid derivative that participates in the coupling reaction with aryl halides or vinyl halides, leading to the formation of biaryl or vinyl compounds.Additionally, $name$ can be used in the preparation of heterocyclic compounds, pharmaceutical intermediates, and functional materials. Its ability to undergo selective and efficient cross-coupling reactions makes it a valuable tool in the synthesis of diverse chemical structures with tailored properties.In summary, the application of 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyridinecarbonitrile is instrumental in organic synthesis for the construction of complex molecules, making it an essential reagent for chemists and researchers working in the field of chemical synthesis.
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