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AA53932

1217501-00-2 | 4-(1-Cyanocyclopropyl)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $22.00 $16.00 -   +
250mg 98% in stock $45.00 $32.00 -   +
1g 98% in stock $60.00 $42.00 -   +
5g 98% in stock $264.00 $185.00 -   +
10g 98% in stock $528.00 $370.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA53932
Chemical Name: 4-(1-Cyanocyclopropyl)phenylboronic acid
CAS Number: 1217501-00-2
Molecular Formula: C10H10BNO2
Molecular Weight: 187.0029
MDL Number: MFCD12546546
SMILES: OB(c1ccc(cc1)C1(CC1)C#N)O

 

Computed Properties
Complexity: 259  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 14  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • The (4-(1-Cyanocyclopropyl)phenyl)boronic acid is a versatile compound widely used in chemical synthesis. Its unique structure allows for a variety of applications in organic chemistry, particularly in the formation of carbon-carbon and carbon-heteroatom bonds.One key application of this compound is in Suzuki-Miyaura coupling reactions, where it serves as a vital component for the cross-coupling of organic halides or pseudohalides with aryl boronic acids. This reaction is highly valuable in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and materials.Furthermore, the (4-(1-Cyanocyclopropyl)phenyl)boronic acid can also be employed in the construction of functionalized cyclopropane derivatives through C-H activation reactions. This allows for the rapid and efficient generation of molecular complexity, enabling the synthesis of bioactive compounds and natural products.Overall, the (4-(1-Cyanocyclopropyl)phenyl)boronic acid is a powerful tool in the hands of synthetic chemists, offering diverse opportunities for the assembly of structurally complex molecules with high efficiency and selectivity.
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