AA04330
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $8.00 | $5.00 | - + | |
1g | 97% | in stock | $9.00 | $7.00 | - + | |
5g | 97% | in stock | $39.00 | $28.00 | - + | |
25g | 97% | in stock | $179.00 | $125.00 | - + | |
100g | 97% | in stock | $595.00 | $416.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA04330 |
Chemical Name: | (6-Phenyldibenzo[b,d]furan-4-yl)boronic acid |
CAS Number: | 1010068-85-5 |
Molecular Formula: | C18H13BO3 |
Molecular Weight: | 288.10502 |
MDL Number: | MFCD29077673 |
SMILES: | OB(c1cccc2c1oc1c2cccc1c1ccccc1)O |
6-Phenyldibenzofuran-4-boronic acid is a vital building block in chemical synthesis, particularly in the field of organic chemistry. This compound serves as a versatile reagent in various reactions due to its boronic acid functionality, which enables it to participate in Suzuki-Miyaura cross-coupling reactions. By reacting with appropriate partners such as aryl halides or triflates in the presence of palladium catalysts, this boronic acid derivative can facilitate the formation of biaryl compounds, which are prevalent structural motifs in many natural products and pharmaceuticals. Additionally, 6-Phenyldibenzofuran-4-boronic acid can also be utilized in the construction of more complex molecules through sequential coupling reactions, allowing for the rapid assembly of diverse molecular architectures with high efficiency and selectivity. Its broad synthetic utility and compatibility with various functional groups make it a valuable tool for chemists engaged in the synthesis of novel organic compounds for applications in drug discovery, materials science, and other research fields.