AA01514
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.
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 |
Complexity: | 369 |
Covalently-Bonded Unit Count: | 3 |
Heavy Atom Count: | 39 |
Hydrogen Bond Acceptor Count: | 10 |
Rotatable Bond Count: | 8 |
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.