N-[(1S,2S)-2-aMino-1,2-diphenylethyl]-BenzenesulfonaMide
98%
- Product Code: 70721
CAS:
300345-91-9
| Molecular Weight: | 352.45 g./mol | Molecular Formula: | C₂₀H₂₀N₂O₂S |
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| 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 various organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a benzenesulfonamide group and chiral centers, makes it effective in controlling stereochemistry during reactions such as hydrogenation, alkylation, or cyclization. It is also employed in the development of pharmaceuticals, particularly in the synthesis of chiral drugs, where precise stereochemistry is crucial for biological activity. Additionally, it finds use in academic research for studying enantioselective transformations and developing new catalytic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | ฿4,392.00 |
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| 1.000 | 10-20 days | ฿13,014.00 |
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N-[(1S,2S)-2-aMino-1,2-diphenylethyl]-BenzenesulfonaMide
This compound is primarily utilized in the field of asymmetric synthesis and catalysis. It serves as a chiral auxiliary or ligand in various organic reactions, enabling the production of enantiomerically pure compounds. Its structure, featuring a benzenesulfonamide group and chiral centers, makes it effective in controlling stereochemistry during reactions such as hydrogenation, alkylation, or cyclization. It is also employed in the development of pharmaceuticals, particularly in the synthesis of chiral drugs, where precise stereochemistry is crucial for biological activity. Additionally, it finds use in academic research for studying enantioselective transformations and developing new catalytic methodologies.
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