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741709-58-0

2-ACETYLPYRIDINE-4-BORONIC ACID PINACOL ESTER

Catalog#: AR00FETB  |   CAS#: 741709-58-0  |   MDL#: MFCD09952047  |   MF: C13H18BNO3  |   MW: 247.09792

Packsize Purity Price Availability Quantity
100mg 97% $56.00 Global Stock Buy Now Add To Cart
250mg 97% $84.00 Global Stock Buy Now Add To Cart
1g 97% $212.00 Global Stock Buy Now Add To Cart
5g 97% $751.00 Global Stock Buy Now Add To Cart
25g 97% $2,476.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00FETB
Chemical Name 2-ACETYLPYRIDINE-4-BORONIC ACID PINACOL ESTER
CAS Number 741709-58-0
Molecular Formula C13H18BNO3
Molecular Weight 247.09792
MDL Number MFCD09952047
SMILES CC(=O)c1nccc(c1)B1OC(C(O1)(C)C)(C)C

1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)ethanone is a versatile compound that finds extensive application in chemical synthesis, particularly in the field of organic chemistry. Due to its unique structural properties, this compound serves as a valuable building block for the synthesis of complex molecules and pharmaceutical intermediates.In organic synthesis, 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)ethanone is commonly employed as a functional group manipulator. Its reactivity allows for the selective modification of other molecules, enabling chemists to introduce specific functionalities at desired positions within a target compound. This controlled functionalization is crucial in the development of new drugs, agrochemicals, and materials with tailored properties.Furthermore, the presence of the boron-containing moiety in 1-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)ethanone imparts unique characteristics to the molecules into which it is incorporated. Boron-containing compounds often exhibit enhanced stability, reactivity, and selectivity in various chemical reactions, making them valuable tools in modern synthetic chemistry. Therefore, the strategic placement of this compound in a synthetic route can facilitate the efficient construction of complex molecular architectures with defined stereochemistry and functionality.
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