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AA20015

1150114-44-5 | 5-(Ethoxycarbonyl)furan-2-boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $13.00 $9.00 -   +
250mg 98% in stock $20.00 $14.00 -   +
1g 98% in stock $60.00 $42.00 -   +
5g 98% in stock $290.00 $203.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA20015
Chemical Name: 5-(Ethoxycarbonyl)furan-2-boronic acid
CAS Number: 1150114-44-5
Molecular Formula: C7H9BO5
Molecular Weight: 183.95436000000007
MDL Number: MFCD10696632
SMILES: CCOC(=O)c1ccc(o1)B(O)O

 

Computed Properties
Complexity: 184  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 4  

 

 

Upstream Synthesis Route
  • The (5-(Ethoxycarbonyl)furan-2-yl)boronic acid, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique properties and reactivity. This compound is commonly utilized in organic reactions, particularly in the field of cross-coupling reactions for the formation of carbon-carbon and carbon-heteroatom bonds.One of the key applications of $name$ is its involvement in Suzuki-Miyaura cross-coupling reactions, where it can react with various aryl halides or pseudohalides to yield biaryl compounds. This reaction is widely used in the synthesis of pharmaceuticals, agrochemicals, and materials science.Additionally, $name$ can participate in palladium-catalyzed C-H activation reactions to functionalize aromatic compounds, enabling the introduction of a variety of functional groups at specific positions in the molecule. This allows for the rapid and efficient construction of complex organic molecules with high selectivity.Moreover, $name$ can be employed in the synthesis of heterocyclic compounds, which are important structural motifs found in many biologically active molecules. By utilizing the boronic acid functionality of $name$, chemists can access a diverse range of heterocycles with tailored properties for various applications in medicinal chemistry and materials science.In conclusion, the (5-(Ethoxycarbonyl)furan-2-yl)boronic acid, or $name$, plays a crucial role in modern chemical synthesis by enabling the construction of complex organic molecules with high efficiency and selectivity. Its versatile reactivity and compatibility with various catalytic systems make it a valuable tool for synthetic chemists in the development of new materials and bioactive compounds.
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