N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide
≥98%,≥99% e.e.
- Product Code: 71235
CAS:
852212-89-6
| Molecular Weight: | 344.4 g./mol | Molecular Formula: | C₁₅H₁₅F₃N₂O₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | 174-176°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or catalyst. Its unique structure, featuring a trifluoromethanesulfonamide group and a diphenylethyl backbone, makes it effective in facilitating enantioselective reactions. It is often employed in the synthesis of complex organic molecules, particularly in the pharmaceutical industry, where the production of enantiomerically pure drugs is critical. Additionally, its stability and reactivity under various conditions make it a valuable tool in organic chemistry research, enabling the development of novel synthetic pathways and methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿1,030.00 |
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| 1.000 | 10-20 days | ฿3,040.00 |
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N-[(1R,2R)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide
This compound is primarily utilized in the field of asymmetric synthesis, where it serves as a chiral auxiliary or catalyst. Its unique structure, featuring a trifluoromethanesulfonamide group and a diphenylethyl backbone, makes it effective in facilitating enantioselective reactions. It is often employed in the synthesis of complex organic molecules, particularly in the pharmaceutical industry, where the production of enantiomerically pure drugs is critical. Additionally, its stability and reactivity under various conditions make it a valuable tool in organic chemistry research, enabling the development of novel synthetic pathways and methodologies.
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