(S)-1-[(S)-1-(Di-tert-butylphosphino)ethyl]-2-[(S)-phenylphosphinoyl]ferrocene
98%
- Product Code: 68670
CAS:
1221746-66-2
| Molecular Weight: | 482.37 g./mol | Molecular Formula: | C₂₆H₃₆FeOP₂ |
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| EC Number: | MDL Number: | MFCD19105637 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating a ferrocene backbone and chiral phosphine groups, makes it highly effective in inducing enantioselectivity. It is widely applied in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial. For example, it is employed in asymmetric hydrogenation reactions to produce chiral intermediates for drugs. Its robustness and ability to maintain high enantiomeric excess under various conditions make it a valuable tool in organic synthesis. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereoselective transformations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.050 | 10-20 days | $238.67 |
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| 0.100 | 10-20 days | $451.13 |
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| 0.250 | 10-20 days | $895.03 |
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(S)-1-[(S)-1-(Di-tert-butylphosphino)ethyl]-2-[(S)-phenylphosphinoyl]ferrocene
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating a ferrocene backbone and chiral phosphine groups, makes it highly effective in inducing enantioselectivity. It is widely applied in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial. For example, it is employed in asymmetric hydrogenation reactions to produce chiral intermediates for drugs. Its robustness and ability to maintain high enantiomeric excess under various conditions make it a valuable tool in organic synthesis. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereoselective transformations.
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