(R)-1-[(R)-2-[Bis[4-(trifluoromethyl)phenyl]phosphino]ferrocenyl]ethylbis[4-(trifluoromethyl)phenyl]phosphine
97%
- Product Code: 37374
CAS:
166172-60-7
| Molecular Weight: | 854.4200 g./mol | Molecular Formula: | C₄₀H₂₈F₁₂FeP₂ |
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| Density: | Storage Condition: | 2-8°C |
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 trifluoromethylphenyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is especially effective in synthesizing pharmaceuticals and fine chemicals where high enantiomeric purity is critical. The trifluoromethyl groups improve the ligand's electron-withdrawing properties, making it suitable for reactions requiring precise control over reactivity and selectivity. Its application extends to industrial and academic research for developing advanced catalytic systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $122.95 |
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(R)-1-[(R)-2-[Bis[4-(trifluoromethyl)phenyl]phosphino]ferrocenyl]ethylbis[4-(trifluoromethyl)phenyl]phosphine
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and trifluoromethylphenyl groups, enhances stereoselectivity in processes such as hydrogenation, carbon-carbon bond formation, and other enantioselective transformations. It is especially effective in synthesizing pharmaceuticals and fine chemicals where high enantiomeric purity is critical. The trifluoromethyl groups improve the ligand's electron-withdrawing properties, making it suitable for reactions requiring precise control over reactivity and selectivity. Its application extends to industrial and academic research for developing advanced catalytic systems.
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