(S)-1-[(Rp)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine
97%
- Product Code: 70454
CAS:
277306-29-3
| Molecular Weight: | 542.45 g./mol | Molecular Formula: | C₃₂H₄₀FeP₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01074443 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in the synthesis of enantiomerically pure compounds, which are essential in the pharmaceutical industry for producing drugs with high stereoselectivity. It is often employed in hydrogenation, cross-coupling, and allylic substitution reactions, where it enhances the efficiency and selectivity of the catalytic process. Its ferrocene backbone and bulky tert-butyl groups contribute to its stability and ability to induce high enantioselectivity in complex organic transformations. Additionally, it is utilized in academic and industrial research for developing new catalytic methodologies and optimizing synthetic routes for chiral molecules.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| Appearance | Orange powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿620.00 |
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(S)-1-[(Rp)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine
This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in the synthesis of enantiomerically pure compounds, which are essential in the pharmaceutical industry for producing drugs with high stereoselectivity. It is often employed in hydrogenation, cross-coupling, and allylic substitution reactions, where it enhances the efficiency and selectivity of the catalytic process. Its ferrocene backbone and bulky tert-butyl groups contribute to its stability and ability to induce high enantioselectivity in complex organic transformations. Additionally, it is utilized in academic and industrial research for developing new catalytic methodologies and optimizing synthetic routes for chiral molecules.
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