N-[(1R,2R)-2-aMino-1,2-diphenylethyl]-4-(trifluoroMethyl)-BenzenesulfonaMide
98%
- Product Code: 70688
CAS:
1105576-13-3
| Molecular Weight: | 420.4479696 g./mol | Molecular Formula: | C₂₁H₁₉F₃N₂O₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, away from light |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral auxiliary or ligand in organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a trifluoromethyl group and a benzenesulfonamide moiety, enhances its effectiveness in stereoselective transformations, particularly in the synthesis of pharmaceuticals and fine chemicals. The compound's ability to induce high enantioselectivity makes it valuable in the development of active pharmaceutical ingredients (APIs) where chirality plays a critical role in biological activity. Additionally, it is used in research to explore new catalytic processes and optimize existing methodologies for industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿400.00 |
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| 0.250 | 10-20 days | ฿1,780.00 |
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| 1.000 | 10-20 days | ฿4,560.00 |
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N-[(1R,2R)-2-aMino-1,2-diphenylethyl]-4-(trifluoroMethyl)-BenzenesulfonaMide
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral auxiliary or ligand in organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a trifluoromethyl group and a benzenesulfonamide moiety, enhances its effectiveness in stereoselective transformations, particularly in the synthesis of pharmaceuticals and fine chemicals. The compound's ability to induce high enantioselectivity makes it valuable in the development of active pharmaceutical ingredients (APIs) where chirality plays a critical role in biological activity. Additionally, it is used in research to explore new catalytic processes and optimize existing methodologies for industrial applications.
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