(3aS,6aS)-rel-tert-Butyl hexahydropyrrolo[3,4-b]pyrrole-1(2H)-carboxylate
98%
- Product Code: 70898
CAS:
1018443-32-7
| Molecular Weight: | 212.29 g./mol | Molecular Formula: | C₁₁H₂₀N₂O₂ |
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| EC Number: | MDL Number: | MFCD12198661 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules, particularly in pharmaceutical research. Its structure is valuable for constructing pyrrolidine-based frameworks, which are commonly found in bioactive compounds. The tert-butyl group enhances stability and facilitates selective reactions, making it useful in the development of drug candidates targeting various diseases. Additionally, its stereochemistry allows for the creation of chiral molecules, which are critical in designing enantioselective drugs. Researchers also employ it in the synthesis of natural products and heterocyclic compounds, leveraging its versatility in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,300.00 |
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| 0.250 | 10-20 days | ฿10,647.00 |
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| 1.000 | 10-20 days | ฿24,885.00 |
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(3aS,6aS)-rel-tert-Butyl hexahydropyrrolo[3,4-b]pyrrole-1(2H)-carboxylate
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of complex molecules, particularly in pharmaceutical research. Its structure is valuable for constructing pyrrolidine-based frameworks, which are commonly found in bioactive compounds. The tert-butyl group enhances stability and facilitates selective reactions, making it useful in the development of drug candidates targeting various diseases. Additionally, its stereochemistry allows for the creation of chiral molecules, which are critical in designing enantioselective drugs. Researchers also employ it in the synthesis of natural products and heterocyclic compounds, leveraging its versatility in multi-step synthetic routes.
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