rel-tert-Butyl (3aS,8aS)-octahydro-6H-isothiazolo[4,5-d]azepine-6-carboxylate 1,1-dioxide
95%
- Product Code: 124516
CAS:
1263181-13-0
| Molecular Weight: | 290.38 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₄S |
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| EC Number: | MDL Number: | MFCD21362258 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an isothiazole and azepine ring system, makes it valuable for developing compounds with potential therapeutic applications. It is often employed in the design and production of protease inhibitors, which are critical in treating diseases such as viral infections and certain types of cancer. Additionally, its unique stereochemistry and functional groups allow for precise modifications, enabling researchers to optimize drug candidates for enhanced efficacy and selectivity. The compound is also explored in the development of novel anti-inflammatory and neuroprotective agents, leveraging its ability to interact with specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,515.97 |
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rel-tert-Butyl (3aS,8aS)-octahydro-6H-isothiazolo[4,5-d]azepine-6-carboxylate 1,1-dioxide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring an isothiazole and azepine ring system, makes it valuable for developing compounds with potential therapeutic applications. It is often employed in the design and production of protease inhibitors, which are critical in treating diseases such as viral infections and certain types of cancer. Additionally, its unique stereochemistry and functional groups allow for precise modifications, enabling researchers to optimize drug candidates for enhanced efficacy and selectivity. The compound is also explored in the development of novel anti-inflammatory and neuroprotective agents, leveraging its ability to interact with specific biological targets.
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