(S)-1-((Rp)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenyl)ethyldi-tert-butylphosphine
98%
- Product Code: 70438
CAS:
849924-40-9
| Molecular Weight: | 658.61 g./mol | Molecular Formula: | C₃₈H₅₂FeO₂P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08561157 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, combining ferrocene and phosphine groups, provides excellent steric and electronic control, leading to high enantiomeric excess in the synthesis of chiral molecules. This makes it valuable in the pharmaceutical industry for producing enantiomerically pure drugs and intermediates. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore asymmetric synthesis pathways.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| Appearance | Orange powder |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €176.23 |
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(S)-1-((Rp)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenyl)ethyldi-tert-butylphosphine
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, combining ferrocene and phosphine groups, provides excellent steric and electronic control, leading to high enantiomeric excess in the synthesis of chiral molecules. This makes it valuable in the pharmaceutical industry for producing enantiomerically pure drugs and intermediates. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore asymmetric synthesis pathways.
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