N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-2,3,4,5,6-pentafluorobenzenesulfonamide
≥98%
- Product Code: 71241
CAS:
313342-24-4
| Molecular Weight: | 442.4 g./mol | Molecular Formula: | C₂₀H₁₅F₅N₂O₂S |
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| EC Number: | MDL Number: | ||
| Melting Point: | 196-198°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 organic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a pentafluorobenzenesulfonamide group and a chiral diamine backbone, makes it effective in inducing high enantioselectivity in reactions such as hydrogenations, aldol additions, and other carbon-carbon bond-forming processes. Additionally, it is employed in pharmaceutical research for the development of chiral drugs, where precise control over stereochemistry is crucial for efficacy and safety. Its robust and versatile nature also makes it suitable for use in material science, particularly in the design of chiral polymers or supramolecular assemblies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,680.00 |
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N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-2,3,4,5,6-pentafluorobenzenesulfonamide
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral ligand or catalyst in various organic reactions, particularly in the synthesis of enantiomerically pure compounds. Its unique structure, featuring a pentafluorobenzenesulfonamide group and a chiral diamine backbone, makes it effective in inducing high enantioselectivity in reactions such as hydrogenations, aldol additions, and other carbon-carbon bond-forming processes. Additionally, it is employed in pharmaceutical research for the development of chiral drugs, where precise control over stereochemistry is crucial for efficacy and safety. Its robust and versatile nature also makes it suitable for use in material science, particularly in the design of chiral polymers or supramolecular assemblies.
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