[S(R)]-N-[(S)-[4-(1,1-Dimethylethyl)phenyl][5-(diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]methyl]-2-methyl-2-propanesulfinamide
95%
- Product Code: 65344
CAS:
2160535-59-9
| Molecular Weight: | 659.9 g./mol | Molecular Formula: | C₄₂H₄₆NO₂PS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32697186 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
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 xanthene backbone and a sulfinamide group, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in asymmetric hydrogenation, C-C bond formation, and other stereoselective processes, enabling the synthesis of complex chiral molecules with high optical purity. Its application is particularly valuable in the pharmaceutical industry for producing enantiomerically pure active pharmaceutical ingredients (APIs) and intermediates. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring stereochemical outcomes in synthetic chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿1,791.00 |
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| 0.025 | 10-20 days | ฿8,091.00 |
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| 0.100 | 10-20 days | ฿23,391.00 |
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[S(R)]-N-[(S)-[4-(1,1-Dimethylethyl)phenyl][5-(diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]methyl]-2-methyl-2-propanesulfinamide
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a xanthene backbone and a sulfinamide group, makes it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in asymmetric hydrogenation, C-C bond formation, and other stereoselective processes, enabling the synthesis of complex chiral molecules with high optical purity. Its application is particularly valuable in the pharmaceutical industry for producing enantiomerically pure active pharmaceutical ingredients (APIs) and intermediates. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring stereochemical outcomes in synthetic chemistry.
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