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AE10436

1031747-48-4 | 3-(N-Cyclopropylaminocarbonyl)methylphenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $105.00 $73.00 -   +
1g 96% in stock $267.00 $187.00 -   +
5g 96% in stock $760.00 $532.00 -   +

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*All prices are in USD.

Description
Catalog Number: AE10436
Chemical Name: 3-(N-Cyclopropylaminocarbonyl)methylphenylboronic acid, pinacol ester
CAS Number: 1031747-48-4
Molecular Formula: C17H24BNO3
Molecular Weight: 301.18836
MDL Number: MFCD17015829
SMILES: O=C(Cc1cccc(c1)B1OC(C(O1)(C)C)(C)C)NC1CC1

 

Computed Properties
Complexity: 418  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 22  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • 3-(N-Cyclopropylaminocarbonyl)methylphenylboronic acid, pinacol ester is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. This compound is commonly employed as a key building block in the synthesis of pharmaceuticals, agrochemicals, and materials due to its ability to facilitate diverse chemical transformations.In chemical synthesis, 3-(N-Cyclopropylaminocarbonyl)methylphenylboronic acid, pinacol ester serves as a valuable reagent for the Suzuki-Miyaura cross-coupling reaction, a powerful tool for forming carbon-carbon bonds. By participating in this reaction, the compound enables the construction of complex molecular structures with high efficiency and selectivity, making it an indispensable tool for medicinal chemists and synthetic organic chemists.Furthermore, the pinacol ester group in 3-(N-Cyclopropylaminocarbonyl)methylphenylboronic acid provides stability and solubility, allowing for increased versatility in reaction conditions and compatibility with a variety of functional groups. This feature enhances the compound's utility in a wide range of synthetic processes, including the preparation of bioactive molecules and advanced materials.Overall, 3-(N-Cyclopropylaminocarbonyl)methylphenylboronic acid, pinacol ester plays a crucial role in chemical synthesis by facilitating the creation of complex chemical structures and enabling the development of new molecules with potential applications in various fields.
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