AA02710
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 96% | in stock | $106.00 | $75.00 | - + | |
5g | 96% | in stock | $299.00 | $209.00 | - + | |
25g | 96% | in stock | $760.00 | $532.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA02710 |
Chemical Name: | 4-Benzylthiophenylboronic acid |
CAS Number: | 1005207-32-8 |
Molecular Formula: | C13H13BO2S |
Molecular Weight: | 244.1171 |
MDL Number: | MFCD06801692 |
SMILES: | OB(c1ccc(cc1)SCc1ccccc1)O |
Complexity: | 212 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 17 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 4 |
In chemical synthesis, (4-(Benzylthio)phenyl)boronic acid, also known as $name$, serves as a versatile building block for creating a wide range of organic compounds. Its unique structure offers a valuable platform for forming carbon-carbon and carbon-heteroatom bonds, making it a crucial reagent in various transformations.Due to its boronic acid functionality, $name$ can participate in Suzuki-Miyaura cross-coupling reactions, enabling the creation of biaryl linkages. This process is widely used in medicinal chemistry, material science, and natural product synthesis. By coupling with various aryl halides or pseudohalides, (4-(Benzylthio)phenyl)boronic acid facilitates the construction of complex molecules with high efficiency and selectivity.Furthermore, the thioether group in the molecule provides an additional handle for introducing sulfur atoms into target molecules. This sulfur-containing motif can offer unique properties to the final compounds, enhancing their biological activity or material characteristics.Overall, (4-(Benzylthio)phenyl)boronic acid plays a crucial role as a versatile synthetic building block in the preparation of diverse organic compounds with applications in drug discovery, materials science, and chemical research.