AA20015
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.
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 |
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 |
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.