tert-Butyl 3-(acetylthio)azetidine-1-carboxylate
95%
- Product Code: 83546
CAS:
183800-74-0
| Molecular Weight: | 231.31 g./mol | Molecular Formula: | C₁₀H₁₇NO₃S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile intermediate. It is particularly valuable in the development of pharmaceuticals and bioactive molecules due to its azetidine ring, which is a key structural motif in many drug candidates. The tert-butyl group provides steric protection, enhancing stability during synthetic processes, while the acetylthio moiety allows for further functionalization through thiol chemistry. Its application is prominent in the synthesis of compounds targeting neurological disorders, cancer, and infectious diseases, where azetidine derivatives play a crucial role. Additionally, it serves as a building block in the preparation of peptidomimetics and other complex organic molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow To Red To Brown Liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €480.15 |
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| 1.000 | 10-20 days | €1,020.98 |
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tert-Butyl 3-(acetylthio)azetidine-1-carboxylate
This compound is primarily utilized in organic synthesis as a versatile intermediate. It is particularly valuable in the development of pharmaceuticals and bioactive molecules due to its azetidine ring, which is a key structural motif in many drug candidates. The tert-butyl group provides steric protection, enhancing stability during synthetic processes, while the acetylthio moiety allows for further functionalization through thiol chemistry. Its application is prominent in the synthesis of compounds targeting neurological disorders, cancer, and infectious diseases, where azetidine derivatives play a crucial role. Additionally, it serves as a building block in the preparation of peptidomimetics and other complex organic molecules.
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