1,1'-Bis(dicyclohexylphosphino)ferrocene
97%
- Product Code: 126671
Alias:
1,1'-Bis(dicyclohexylphosphine)-ferrocene
CAS:
146960-90-9
| Molecular Weight: | 578.57 g./mol | Molecular Formula: | C₃₄H₅₂FeP₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 134-136°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
1,1'-Bis(dicyclohexylphosphino)ferrocene is widely used as a ligand in transition metal catalysis, particularly in asymmetric synthesis and cross-coupling reactions. Its unique ferrocene backbone and bulky dicyclohexylphosphine groups make it highly effective in stabilizing metal complexes and enhancing catalytic activity. It is commonly employed in palladium-catalyzed reactions, such as Suzuki-Miyaura and Heck couplings, where it improves selectivity and yield. Additionally, its chiral derivatives are valuable in enantioselective transformations, including hydrogenation and carbon-carbon bond formation, making it a key component in the synthesis of pharmaceuticals and fine chemicals. The ligand’s robustness and versatility also make it suitable for use in challenging reaction conditions.
Product Specification:
| Test | Specification |
|---|---|
| Carbon | 68.1-73.1 |
| Melting Point | 134-136 |
| Purity (%) | 97-100 |
| Appearance | Orange Powder |
| Infrared Spectrum | Conforms To Structure |
| Proton Nmr Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $14.94 |
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| 1.000 | 10-20 days | $25.96 |
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| 5.000 | 10-20 days | $106.97 |
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| 25.000 | 10-20 days | $491.58 |
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1,1'-Bis(dicyclohexylphosphino)ferrocene
1,1'-Bis(dicyclohexylphosphino)ferrocene is widely used as a ligand in transition metal catalysis, particularly in asymmetric synthesis and cross-coupling reactions. Its unique ferrocene backbone and bulky dicyclohexylphosphine groups make it highly effective in stabilizing metal complexes and enhancing catalytic activity. It is commonly employed in palladium-catalyzed reactions, such as Suzuki-Miyaura and Heck couplings, where it improves selectivity and yield. Additionally, its chiral derivatives are valuable in enantioselective transformations, including hydrogenation and carbon-carbon bond formation, making it a key component in the synthesis of pharmaceuticals and fine chemicals. The ligand’s robustness and versatility also make it suitable for use in challenging reaction conditions.
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