N-((1R,2R)-2-Amino-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide
98%
- Product Code: 70685
CAS:
1020665-67-1
| Molecular Weight: | 488.45 g./mol | Molecular Formula: | C₂₂H₁₈F₆N₂O₂S |
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| Density: | Storage Condition: | 2-8°C, dark, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral catalysts. It is often employed in enantioselective reactions, where it helps in the formation of chiral centers with high selectivity. The presence of trifluoromethyl groups enhances its electron-withdrawing properties, making it effective in stabilizing intermediates during catalytic cycles. Additionally, it is used in the synthesis of complex organic molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Its robust structure and ability to induce high enantiomeric excess make it a valuable tool in the production of optically active compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿990.00 |
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| 0.250 | 10-20 days | ฿3,951.00 |
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N-((1R,2R)-2-Amino-1,2-diphenylethyl)-3,5-bis(trifluoromethyl)benzenesulfonamide
This compound is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral catalysts. It is often employed in enantioselective reactions, where it helps in the formation of chiral centers with high selectivity. The presence of trifluoromethyl groups enhances its electron-withdrawing properties, making it effective in stabilizing intermediates during catalytic cycles. Additionally, it is used in the synthesis of complex organic molecules, including pharmaceuticals, where precise control over stereochemistry is crucial. Its robust structure and ability to induce high enantiomeric excess make it a valuable tool in the production of optically active compounds.
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