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AA53924

1217501-08-0 | 4-(1-(Methoxycarbonyl)cyclopropyl)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $35.00 $25.00 -   +
1g 97% in stock $135.00 $95.00 -   +
25g 97% in stock $3,370.00 $2,359.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA53924
Chemical Name: 4-(1-(Methoxycarbonyl)cyclopropyl)phenylboronic acid
CAS Number: 1217501-08-0
Molecular Formula: C11H13BO4
Molecular Weight: 220.0295
MDL Number: MFCD12546570
SMILES: COC(=O)C1(CC1)c1ccc(cc1)B(O)O

 

Computed Properties
Complexity: 267  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • (4-(1-(Methoxycarbonyl)cyclopropyl)phenyl)boronic acid is a versatile compound commonly utilized in chemical synthesis for the preparation of various organic molecules. With its unique structure containing a boronic acid group attached to a cyclopropyl ring substituted with a methoxycarbonyl group, this compound offers valuable applications in the field of organic chemistry.In chemical synthesis, (4-(1-(Methoxycarbonyl)cyclopropyl)phenyl)boronic acid serves as a key building block for the construction of complex molecules. The boronic acid functionality enables it to participate in important reactions such as Suzuki coupling, which is widely used for the formation of carbon-carbon bonds. By incorporating this compound into synthetic routes, chemists can access a wide range of structurally diverse compounds with potential applications in pharmaceuticals, agrochemicals, materials science, and more.Furthermore, the cyclopropyl ring in the structure of (4-(1-(Methoxycarbonyl)cyclopropyl)phenyl)boronic acid adds an element of rigidity and steric control to the molecules being synthesized. This can influence the stereochemistry and overall three-dimensional shape of the final products, making it a valuable tool for designing and accessing chiral compounds with specific biological or physical properties.Overall, (4-(1-(Methoxycarbonyl)cyclopropyl)phenyl)boronic acid is a versatile and valuable reagent in chemical synthesis, offering chemists the opportunity to explore new synthetic pathways and access a diverse array of organic molecules with tailored properties.
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