AA55926
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 97% | in stock | $25.00 | $17.00 | - + | |
5g | 97% | in stock | $55.00 | $38.00 | - + | |
25g | 97% | in stock | $258.00 | $180.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA55926 |
Chemical Name: | (9,9-Diphenyl-9h-fluoren-4-yl)boronic acid |
CAS Number: | 1224976-40-2 |
Molecular Formula: | C25H19BO2 |
Molecular Weight: | 362.2282 |
MDL Number: | MFCD29077672 |
SMILES: | OB(c1cccc2c1-c1ccccc1C2(c1ccccc1)c1ccccc1)O |
Complexity: | 505 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 28 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Rotatable Bond Count: | 3 |
Derived from the class of boronic acids, (9,9-Diphenyl-9H-fluoren-4-yl)boronic acid is a versatile compound widely utilized in chemical synthesis. Its distinctive structure featuring a boron atom directly bonded to a fluorene scaffold makes it a valuable building block for constructing complex organic molecules. In organic synthesis, this compound serves as a key component for Suzuki-Miyaura cross-coupling reactions, enabling the efficient formation of carbon-carbon bonds. This method is crucial in the assembly of pharmaceuticals, agrochemicals, and materials with tailored properties. Additionally, (9,9-Diphenyl-9H-fluoren-4-yl)boronic acid participates in a range of other transformations, such as hydroboration and metal-catalyzed transformations, empowering chemists to access diverse molecular architectures in their quest for new compounds with unique functions.