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AA20046

1150114-63-8 | 2-Fluoro-6-(trifluoromethyl)pyridine-3-boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $168.00 $117.00 -   +
250mg 95% in stock $288.00 $201.00 -   +
1g 95% in stock $712.00 $498.00 -   +
5g 95% in stock $2,358.00 $1,650.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA20046
Chemical Name: 2-Fluoro-6-(trifluoromethyl)pyridine-3-boronic acid
CAS Number: 1150114-63-8
Molecular Formula: C6H4BF4NO2
Molecular Weight: 208.9061
MDL Number: MFCD12025974
SMILES: OB(c1ccc(nc1F)C(F)(F)F)O

 

Computed Properties
Complexity: 201  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • The (2-Fluoro-6-(trifluoromethyl)pyridin-3-yl)boronic acid is a versatile chemical compound that finds wide application in chemical synthesis. Its unique structure enables it to participate in various organic reactions, making it a valuable building block for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, this compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, where it can be used to introduce the pyridine and boronic acid moieties into a wide range of organic molecules. This allows for the rapid and efficient formation of new carbon-carbon bonds, facilitating the synthesis of complex molecules with high precision and control.Furthermore, (2-Fluoro-6-(trifluoromethyl)pyridin-3-yl)boronic acid can also be utilized in metal-catalyzed C-H activation reactions, enabling the direct functionalization of C-H bonds in organic molecules. This methodology offers a more sustainable and atom-economical approach to chemical synthesis, reducing the number of synthetic steps and overall waste generated.Overall, the (2-Fluoro-6-(trifluoromethyl)pyridin-3-yl)boronic acid plays a crucial role in modern organic synthesis, providing chemists with valuable tools to access diverse chemical space and create novel molecules with enhanced properties.
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