(S)-tert-Butyl 2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)amino)-1-methoxy-2-methyl-3-oxopropyl)pyrrolidine-1-carboxylate
98%
- Product Code: 38066
CAS:
160800-65-7
| Molecular Weight: | 420.5400 g./mol | Molecular Formula: | C₂₃H₃₆N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31694246 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex bioactive molecules. Its structure, featuring multiple chiral centers and functional groups, makes it a valuable building block for the development of enantioselective drugs, particularly those targeting specific biological pathways. It is often employed in the preparation of protease inhibitors and other therapeutic agents that require precise stereochemical control. Additionally, its tert-butyl and carboxylate groups enhance its stability and reactivity, facilitating its use in multi-step organic syntheses. Researchers also leverage its unique properties for studying enzyme interactions and designing novel drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,982.00 |
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(S)-tert-Butyl 2-((1R,2R)-3-(((1S,2R)-1-hydroxy-1-phenylpropan-2-yl)amino)-1-methoxy-2-methyl-3-oxopropyl)pyrrolidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of complex bioactive molecules. Its structure, featuring multiple chiral centers and functional groups, makes it a valuable building block for the development of enantioselective drugs, particularly those targeting specific biological pathways. It is often employed in the preparation of protease inhibitors and other therapeutic agents that require precise stereochemical control. Additionally, its tert-butyl and carboxylate groups enhance its stability and reactivity, facilitating its use in multi-step organic syntheses. Researchers also leverage its unique properties for studying enzyme interactions and designing novel drug candidates with improved efficacy and selectivity.
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