(2S)-1-[(4S)-4,5-dihydro-4-phenyl-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene
97%
- Product Code: 59666
CAS:
291536-01-1
| Molecular Weight: | 515.40 g./mol | Molecular Formula: | C₃₁H₂₆FeNOP |
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| EC Number: | MDL Number: | MFCD30475631 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the field of organic chemistry. Its unique structure, featuring a ferrocene backbone and chiral oxazoline-phosphine ligands, makes it highly effective as a chiral ligand in transition metal-catalyzed reactions. It is commonly employed in asymmetric hydrogenation, a process critical for producing enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it finds application in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, contributing to the development of complex organic molecules with high stereoselectivity. Its versatility and efficiency in promoting enantioselective transformations make it a valuable tool in synthetic organic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | €28.49 |
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| 0.250 | 10-20 days | €113.26 |
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(2S)-1-[(4S)-4,5-dihydro-4-phenyl-2-oxazolyl]-2-(diphenylphosphino)-Ferrocene
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the field of organic chemistry. Its unique structure, featuring a ferrocene backbone and chiral oxazoline-phosphine ligands, makes it highly effective as a chiral ligand in transition metal-catalyzed reactions. It is commonly employed in asymmetric hydrogenation, a process critical for producing enantiomerically pure compounds, which are essential in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it finds application in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, contributing to the development of complex organic molecules with high stereoselectivity. Its versatility and efficiency in promoting enantioselective transformations make it a valuable tool in synthetic organic chemistry.
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