(S)-2-Benzyl-N,N-dimethylaziridine-1-sulfonamide
≥96%
- Product Code: 60141
CAS:
902146-43-4
| Molecular Weight: | 240.32 g./mol | Molecular Formula: | C₁₁H₁₆N₂O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20040341 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring an aziridine ring and a sulfonamide group, makes it valuable for constructing complex molecules with high enantiomeric purity. It is often employed in asymmetric synthesis to introduce chirality into target molecules, particularly in the development of pharmaceuticals. The aziridine ring can act as a reactive site for ring-opening reactions, enabling the formation of new carbon-nitrogen bonds. Additionally, the sulfonamide group enhances stability and can participate in further functionalization. This chemical is particularly useful in the synthesis of biologically active compounds, such as enzyme inhibitors or receptor modulators, where stereochemistry plays a critical role in activity. Its application extends to medicinal chemistry research, where it aids in the discovery and optimization of drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,982.00 |
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| 0.250 | 10-20 days | ฿15,192.00 |
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(S)-2-Benzyl-N,N-dimethylaziridine-1-sulfonamide
This compound is primarily utilized in organic synthesis as a chiral building block. Its structure, featuring an aziridine ring and a sulfonamide group, makes it valuable for constructing complex molecules with high enantiomeric purity. It is often employed in asymmetric synthesis to introduce chirality into target molecules, particularly in the development of pharmaceuticals. The aziridine ring can act as a reactive site for ring-opening reactions, enabling the formation of new carbon-nitrogen bonds. Additionally, the sulfonamide group enhances stability and can participate in further functionalization. This chemical is particularly useful in the synthesis of biologically active compounds, such as enzyme inhibitors or receptor modulators, where stereochemistry plays a critical role in activity. Its application extends to medicinal chemistry research, where it aids in the discovery and optimization of drug candidates.
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