(S)-1-[(R)-2-(DI-TERT.-BUTYLPHOSPHINO)FERROCENYL]ETHYLBIS(2-METHYLPHENYL)PHOSPHI
97%
- Product Code: 37962
CAS:
849924-77-2
| Molecular Weight: | 570.515 g./mol | Molecular Formula: | C₂₉H₃₉P₂C₅H₅Fe |
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| EC Number: | MDL Number: | MFCD08561173 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, airtight, dry |
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 sterically demanding phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high optical purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitutions, enabling the creation of complex organic compounds with precise stereochemical control. Its robustness and efficiency make it a valuable tool in organic synthesis and industrial processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,480.00 |
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| 0.250 | 10-20 days | ฿10,440.00 |
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| 1.000 | 10-20 days | ฿26,352.00 |
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(S)-1-[(R)-2-(DI-TERT.-BUTYLPHOSPHINO)FERROCENYL]ETHYLBIS(2-METHYLPHENYL)PHOSPHI
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 sterically demanding phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high optical purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitutions, enabling the creation of complex organic compounds with precise stereochemical control. Its robustness and efficiency make it a valuable tool in organic synthesis and industrial processes.
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