N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide
≥95%,≥99%e.e.
- Product Code: 71239
CAS:
167316-28-1
| Molecular Weight: | 344.4 g./mol | Molecular Formula: | C₁₅H₁₅F₃N₂O₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | 151-153°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand or catalyst in various enantioselective reactions, enabling the production of optically active compounds. Its application is particularly significant in pharmaceutical research, where it aids in the synthesis of chiral drugs with high enantiomeric purity. Additionally, it is employed in organic chemistry for the development of complex molecules with specific stereochemical configurations. Its trifluoromethanesulfonamide group enhances its reactivity and stability, making it a valuable tool in advanced synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,780.00 |
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| 1.000 | 10-20 days | ฿11,290.00 |
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N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-1,1,1-trifluoromethanesulfonamide
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand or catalyst in various enantioselective reactions, enabling the production of optically active compounds. Its application is particularly significant in pharmaceutical research, where it aids in the synthesis of chiral drugs with high enantiomeric purity. Additionally, it is employed in organic chemistry for the development of complex molecules with specific stereochemical configurations. Its trifluoromethanesulfonamide group enhances its reactivity and stability, making it a valuable tool in advanced synthetic methodologies.
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