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Home  > Chemistry  > Organic Building Blocks  > Trifluoromethyls  > 3-Cyano-5-(trifluoromethyl)phenylboronic acid

AD31536

1212021-62-9 | 3-Cyano-5-(trifluoromethyl)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $60.00 $42.00 -   +
250mg 97% in stock $90.00 $63.00 -   +
1g 97% in stock $171.00 $120.00 -   +
5g 97% in stock $573.00 $402.00 -   +
10g 97% in stock $946.00 $662.00 -   +
25g 97% in stock $1,879.00 $1,316.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD31536
Chemical Name: 3-Cyano-5-(trifluoromethyl)phenylboronic acid
CAS Number: 1212021-62-9
Molecular Formula: C8H5BF3NO2
Molecular Weight: 214.937
MDL Number: MFCD03095102
SMILES: N#Cc1cc(cc(c1)C(F)(F)F)B(O)O

 

Computed Properties
Complexity: 273  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • The compound (3-Cyano-5-(trifluoromethyl)phenyl)boronic acid plays a crucial role in chemical synthesis as a versatile building block and reagent. Known for its unique properties, this compound is utilized in various organic reactions to introduce the cyano group, trifluoromethyl group, and boronic acid functionality simultaneously. In organic synthesis, (3-Cyano-5-(trifluoromethyl)phenyl)boronic acid serves as a valuable precursor for the preparation of complex molecules with diverse applications. It can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds efficiently. This compound can also undergo transformation into various functional groups through a range of chemical reactions, contributing to the synthesis of pharmaceuticals, agrochemicals, and materials with tailored properties.Furthermore, (3-Cyano-5-(trifluoromethyl)phenyl)boronic acid exhibits excellent stability and compatibility with a wide range of reaction conditions, making it a preferred choice for chemists aiming to introduce specific functionalities into their target molecules. Its strategic position as a boronic acid derivative allows for selective modifications and strategic manipulations in the synthesis of complex organic compounds.Overall, the application of (3-Cyano-5-(trifluoromethyl)phenyl)boronic acid in chemical synthesis showcases its significance as a valuable tool for the construction of molecular architectures with precision and efficiency.
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