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Home  > 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate)

AA01514

1002345-50-7 | 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate)

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $8.00 $5.00 -   +
1g 97% in stock $9.00 $7.00 -   +
5g 97% in stock $23.00 $17.00 -   +
10g 97% in stock $34.00 $24.00 -   +
25g 97% in stock $84.00 $59.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA01514
Chemical Name: 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate)
CAS Number: 1002345-50-7
Molecular Formula: C27H50B2F8P2
Molecular Weight: 610.2426
MDL Number: MFCD12545948
SMILES: C(CP(C1CCCCC1)C1CCCCC1)CP(C1CCCCC1)C1CCCCC1.F[B-](F)(F)F.F[B-](F)(F)F

 

Computed Properties
Complexity: 369  
Covalently-Bonded Unit Count: 3  
Heavy Atom Count: 39  
Hydrogen Bond Acceptor Count: 10  
Rotatable Bond Count: 8  

 

 

Upstream Synthesis Route
  • 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate) is a versatile and highly effective ligand commonly used in chemical synthesis. This compound is known for its ability to form stable complexes with various transition metals, which play a crucial role in catalyzing a wide range of chemical reactions.In organic synthesis, this ligand is often employed in transition metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura, Heck, and Sonogashira reactions. These reactions are essential in the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The presence of the dicyclohexylphosphino groups in the ligand structure enhances its steric and electronic properties, enabling precise control over the selectivity and efficiency of these catalytic processes.Moreover, the tetrafluoroborate counterions in the compound contribute to its solubility in common organic solvents, making it easier to handle and manipulate in various reaction conditions. Overall, the use of 1,3-Bis(dicyclohexylphosphino)propane bis(tetrafluoroborate) as a ligand in chemical synthesis demonstrates its significant impact on advancing the field of organic chemistry and promoting the development of novel synthetic methodologies.
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