(R)-1-((Sp)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]ferrocenyl)ethyldicyclohexylphosphine
97%
- Product Code: 65705
CAS:
292638-88-1
| Molecular Weight: | 866.52 g./mol | Molecular Formula: | C₄₀H₄₀F₁₂FeP₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08561149 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and bulky, electron-withdrawing trifluoromethyl groups, enhances its effectiveness in inducing high enantioselectivity. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other enantioselective transformations, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its robustness and ability to operate under mild reaction conditions further contribute to its widespread application in organic synthesis.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| Appearance | Orange powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,300.00 |
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| 0.500 | 10-20 days | ฿8,490.00 |
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(R)-1-((Sp)-2-[Bis[3,5-bis(trifluoromethyl)phenyl]phosphino]ferrocenyl)ethyldicyclohexylphosphine
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and bulky, electron-withdrawing trifluoromethyl groups, enhances its effectiveness in inducing high enantioselectivity. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other enantioselective transformations, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Its robustness and ability to operate under mild reaction conditions further contribute to its widespread application in organic synthesis.
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