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719268-92-5

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

Catalog#: AR006250  |   CAS#: 719268-92-5  |   MDL#: MFCD07780754  |   MF: C11H15BFNO2  |   MW: 223.0517

Packsize Purity Price Availability Quantity
250mg 97% $7.00 Global Stock Buy Now Add To Cart
1g 97% $16.00 Global Stock Buy Now Add To Cart
5g 97% $75.00 Global Stock Buy Now Add To Cart
25g 97% $338.00 Global Stock Buy Now Add To Cart
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Catalog Number AR006250
Chemical Name 3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
CAS Number 719268-92-5
Molecular Formula C11H15BFNO2
Molecular Weight 223.0517
MDL Number MFCD07780754
SMILES Fc1cncc(c1)B1OC(C(O1)(C)C)(C)C

3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, often referred to simply as $name$, is a versatile compound widely used in chemical synthesis. This compound plays a crucial role in the formation of carbon-carbon bonds, particularly in cross-coupling reactions.One of the key applications of $name$ in chemical synthesis is its use as a boronic acid derivative in Suzuki-Miyaura cross-coupling reactions. In this process, $name$ can react with aryl halides or vinyl halides in the presence of a palladium catalyst to form biaryl or vinylarene compounds. This reaction is highly valuable in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, $name$ can be involved in other types of coupling reactions, such as Heck reactions and Sonogashira reactions, expanding its utility in the construction of complex organic molecules. Its compatibility with various functional groups and its stability make it a preferred reagent in modern synthetic chemistry.In summary, the application of 3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine in chemical synthesis is pivotal for the efficient and selective formation of carbon-carbon bonds, making it a valuable tool for organic chemists working in diverse fields.
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