1,2-Bis(dicyclohexylphosphino)ethane
98%
- Product Code: 113916
Alias:
1, 2-bis(dicyclohexylphosphoryl)-ethane
CAS:
23743-26-2
| Molecular Weight: | 422.61 g./mol | Molecular Formula: | C₆H₁₁₂PCH₂CH₂PC₆H₁₁₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00015521 | |
| Melting Point: | 92.5-96.5 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Primarily utilized as a ligand in catalytic processes, this compound plays a crucial role in facilitating various organic transformations. Its application is particularly significant in the field of homogeneous catalysis, where it enhances the efficiency and selectivity of metal-catalyzed reactions. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are pivotal in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, its robust structure and ability to stabilize metal centers make it valuable in the development of new catalytic systems for polymerization and hydrogenation processes. The compound's unique phosphine groups also contribute to its effectiveness in asymmetric catalysis, enabling the production of chiral compounds with high enantiomeric purity.
Product Specification:
| Test | Specification |
|---|---|
| Carbon | 70.6-77.2 |
| Purity (Neutralization Titration) | 97.5-102.5 |
| Appearance | White To Off-White Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
| NMR (1H-NMR) | Complies |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $219.44 |
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1,2-Bis(dicyclohexylphosphino)ethane
Primarily utilized as a ligand in catalytic processes, this compound plays a crucial role in facilitating various organic transformations. Its application is particularly significant in the field of homogeneous catalysis, where it enhances the efficiency and selectivity of metal-catalyzed reactions. It is often employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, which are pivotal in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Additionally, its robust structure and ability to stabilize metal centers make it valuable in the development of new catalytic systems for polymerization and hydrogenation processes. The compound's unique phosphine groups also contribute to its effectiveness in asymmetric catalysis, enabling the production of chiral compounds with high enantiomeric purity.
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