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Home  > (9,9-Diphenyl-9h-fluoren-4-yl)boronic acid

AA55926

1224976-40-2 | (9,9-Diphenyl-9h-fluoren-4-yl)boronic acid

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.

Description
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

 

Computed Properties
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  

 

 

Upstream Synthesis Route
  • 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.
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