(1S,3aR,6aS)-tert-Butyl octahydrocyclopenta[c]pyrrole-1-carboxylate
98%
- Product Code: 36261
CAS:
714194-68-0
| Molecular Weight: | 211.3000 g./mol | Molecular Formula: | C₁₂H₂₁NO₂ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
(1S,3aR,6aS)-tert-Butyl octahydrocyclopenta[c]pyrrole-1-carboxylate is primarily used as an intermediate in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. Its stereochemistry and functional groups make it a valuable building block for the development of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. The compound's rigid bicyclic structure is often exploited in medicinal chemistry to create molecules with enhanced binding affinity and selectivity for biological targets. Additionally, it serves as a precursor in the production of peptidomimetics, which are used to mimic the structure and function of peptides in drug design. Its tert-butyl ester group provides stability and facilitates further chemical modifications, making it a versatile reagent in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,031.00 |
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(1S,3aR,6aS)-tert-Butyl octahydrocyclopenta[c]pyrrole-1-carboxylate
(1S,3aR,6aS)-tert-Butyl octahydrocyclopenta[c]pyrrole-1-carboxylate is primarily used as an intermediate in the synthesis of complex organic compounds, particularly in the pharmaceutical industry. Its stereochemistry and functional groups make it a valuable building block for the development of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. The compound's rigid bicyclic structure is often exploited in medicinal chemistry to create molecules with enhanced binding affinity and selectivity for biological targets. Additionally, it serves as a precursor in the production of peptidomimetics, which are used to mimic the structure and function of peptides in drug design. Its tert-butyl ester group provides stability and facilitates further chemical modifications, making it a versatile reagent in organic synthesis.
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