N-[(1S)-2-Hydroxy-1-methylethyl]-2-nitrobenzenesulfonamide
≥95%
- Product Code: 121425
CAS:
1351395-66-8
| Molecular Weight: | 260.27 g./mol | Molecular Formula: | C₉H₁₂N₂O₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21064871 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, dry sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a chiral auxiliary or intermediate in the preparation of enantiomerically pure compounds. Its structure, featuring a nitrobenzenesulfonamide group, makes it useful for protecting amines during complex synthetic processes, particularly in the synthesis of pharmaceuticals and bioactive molecules. The chiral center allows for stereoselective reactions, enabling the production of specific enantiomers with desired biological activity. Additionally, it can be employed in the development of peptide-based drugs, where precise stereochemistry is crucial for efficacy. Its role in facilitating asymmetric synthesis contributes to advancements in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿900.00 |
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| 0.250 | 10-20 days | ฿1,350.00 |
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| 1.000 | 10-20 days | ฿3,411.00 |
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| 5.000 | 10-20 days | ฿10,260.00 |
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N-[(1S)-2-Hydroxy-1-methylethyl]-2-nitrobenzenesulfonamide
This compound is primarily utilized in the field of organic synthesis as a chiral auxiliary or intermediate in the preparation of enantiomerically pure compounds. Its structure, featuring a nitrobenzenesulfonamide group, makes it useful for protecting amines during complex synthetic processes, particularly in the synthesis of pharmaceuticals and bioactive molecules. The chiral center allows for stereoselective reactions, enabling the production of specific enantiomers with desired biological activity. Additionally, it can be employed in the development of peptide-based drugs, where precise stereochemistry is crucial for efficacy. Its role in facilitating asymmetric synthesis contributes to advancements in medicinal chemistry and drug discovery.
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