[S(R)]-N-[(S)-[2-(Dicyclohexylphosphanyl)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide
≥95%
- Product Code: 236128
CAS:
2565792-82-5
| Molecular Weight: | 527.75 g./mol | Molecular Formula: | C₃₁H₄₆NO₂PS |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C, avoid light, inert gas storage |
Product Description:
This chiral sulfinamide compound is primarily used as a specialized ligand precursor in asymmetric catalysis. It plays a key role in the synthesis of chiral phosphine-sulfinamide ligands, which are employed in enantioselective transition metal-catalyzed reactions. These reactions are critical in the pharmaceutical industry for producing single-enantiomer compounds, especially in the development of chiral amines and alcohols. The compound’s stereochemistry enables high enantioselectivity in hydrogenation and cross-coupling reactions. Its application is particularly valuable in research and process chemistry for constructing complex organic molecules with defined stereocenters.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5mg | 10-20 days | ฿1,770.00 |
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| 25mg | 10-20 days | ฿7,850.00 |
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| 100mg | 10-20 days | ฿25,110.00 |
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[S(R)]-N-[(S)-[2-(Dicyclohexylphosphanyl)phenyl](4-methoxyphenyl)methyl]-N,2-dimethyl-2-propanesulfinamide
This chiral sulfinamide compound is primarily used as a specialized ligand precursor in asymmetric catalysis. It plays a key role in the synthesis of chiral phosphine-sulfinamide ligands, which are employed in enantioselective transition metal-catalyzed reactions. These reactions are critical in the pharmaceutical industry for producing single-enantiomer compounds, especially in the development of chiral amines and alcohols. The compound’s stereochemistry enables high enantioselectivity in hydrogenation and cross-coupling reactions. Its application is particularly valuable in research and process chemistry for constructing complex organic molecules with defined stereocenters.
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