(R)-N-((S)-1-(2-((tert-Butyldiphenylsilyl)oxy)phenyl)-2-(diphenylphosphino)ethyl)-2-methylpropane-2-sulfinamide
95%
- Product Code: 53881
CAS:
1803239-59-9
| Molecular Weight: | 663.9200 g./mol | Molecular Formula: | C₄₀H₄₆NO₂PSSi |
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| EC Number: | MDL Number: | MFCD32697178 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, enabling the formation of enantiomerically pure products in organic reactions. Its unique structure, featuring both sulfinamide and phosphine groups, makes it particularly effective in transition metal-catalyzed processes, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions. The tert-butyldiphenylsilyl group provides steric protection, enhancing selectivity during catalysis. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates in drug development, ensuring high enantioselectivity and yield. Additionally, its application extends to the preparation of complex natural products and fine chemicals, where precise stereocontrol is critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $261.63 |
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(R)-N-((S)-1-(2-((tert-Butyldiphenylsilyl)oxy)phenyl)-2-(diphenylphosphino)ethyl)-2-methylpropane-2-sulfinamide
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst, enabling the formation of enantiomerically pure products in organic reactions. Its unique structure, featuring both sulfinamide and phosphine groups, makes it particularly effective in transition metal-catalyzed processes, such as asymmetric hydrogenation or carbon-carbon bond-forming reactions. The tert-butyldiphenylsilyl group provides steric protection, enhancing selectivity during catalysis. It is often employed in the pharmaceutical industry for the synthesis of chiral intermediates in drug development, ensuring high enantioselectivity and yield. Additionally, its application extends to the preparation of complex natural products and fine chemicals, where precise stereocontrol is critical.
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