AA06283
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $13.00 | $9.00 | - + | |
5g | 97% | in stock | $26.00 | $18.00 | - + | |
25g | 97% | in stock | $100.00 | $70.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA06283 |
Chemical Name: | 2-Fluoro-3-iodophenylboronic acid |
CAS Number: | 1016231-39-2 |
Molecular Formula: | C6H5BFIO2 |
Molecular Weight: | 265.8166 |
MDL Number: | MFCD05664305 |
SMILES: | OB(c1cccc(c1F)I)O |
Complexity: | 136 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 1 |
(2-Fluoro-3-iodophenyl)boronic acid is a versatile compound that finds extensive application in modern chemical synthesis. As a key building block in organic chemistry, this boronic acid derivative is utilized in the formation of carbon-carbon and carbon-heteroatom bonds through Suzuki-Miyaura cross-coupling reactions. By serving as a valuable tool in the construction of complex molecular architectures, (2-Fluoro-3-iodophenyl)boronic acid plays a crucial role in the development of various pharmaceuticals, agrochemicals, and materials. Its ability to facilitate the introduction of both fluorine and iodine functionalities in organic molecules makes it highly sought after by synthetic chemists aiming to design novel compounds with enhanced biological or physical properties. Additionally, this compound can be employed in the preparation of advanced materials and functionalized polymers, showcasing its significance in the realm of chemical research and innovation.