tert-butyl 5-benzylhexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
98%
- Product Code: 64567
Alias:
tert-Butyl 5-Benzylhexahydropyrrolo[3,4-C]pyrrole-2-carboxylate
CAS:
186202-73-3
| Molecular Weight: | 302.42 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
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 a pyrrolo[3,4-c]pyrrole core, makes it a valuable building block for developing pharmaceutical agents, particularly those targeting neurological disorders and cardiovascular diseases. Researchers often employ it in the design of inhibitors or modulators for specific enzymes or receptors, leveraging its rigid bicyclic framework to enhance binding affinity and selectivity. Additionally, its tert-butyl carboxylate group provides a protective function during multi-step synthetic processes, ensuring stability and ease of further functionalization. Its applications extend to drug discovery programs aimed at identifying novel therapeutic candidates with improved efficacy and safety profiles.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow Oil |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $91.36 |
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| 0.250 | 10-20 days | $290.70 |
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| 1.000 | 10-20 days | $913.64 |
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tert-butyl 5-benzylhexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate
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 a pyrrolo[3,4-c]pyrrole core, makes it a valuable building block for developing pharmaceutical agents, particularly those targeting neurological disorders and cardiovascular diseases. Researchers often employ it in the design of inhibitors or modulators for specific enzymes or receptors, leveraging its rigid bicyclic framework to enhance binding affinity and selectivity. Additionally, its tert-butyl carboxylate group provides a protective function during multi-step synthetic processes, ensuring stability and ease of further functionalization. Its applications extend to drug discovery programs aimed at identifying novel therapeutic candidates with improved efficacy and safety profiles.
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