(RP)-1-Dicyclohexylphosphino-2-[(R)-α-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene
97%
- Product Code: 68658
CAS:
1016985-24-2
| Molecular Weight: | 711.7595 g./mol | Molecular Formula: | C₄₃H₆₃FeNP₂ |
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| EC Number: | MDL Number: | MFCD04117706 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and phosphine groups, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. The chiral environment it creates around the metal center allows for the production of enantiomerically pure compounds, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its application is especially prominent in the development of chiral drugs, where achieving high enantiomeric purity is essential for efficacy and safety. Additionally, it is used in academic and industrial research to explore new catalytic processes and optimize existing ones for improved selectivity and yield.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,605.00 |
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(RP)-1-Dicyclohexylphosphino-2-[(R)-α-(dimethylamino)-2-(dicyclohexylphosphino)benzyl]ferrocene
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and phosphine groups, makes it highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. The chiral environment it creates around the metal center allows for the production of enantiomerically pure compounds, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its application is especially prominent in the development of chiral drugs, where achieving high enantiomeric purity is essential for efficacy and safety. Additionally, it is used in academic and industrial research to explore new catalytic processes and optimize existing ones for improved selectivity and yield.
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