(2S,4S)-1-Benzyl 2-methyl 4-((tert-butoxycarbonyl)amino)pyrrolidine-1,2-dicarboxylate
97%
- Product Code: 70872
CAS:
168263-80-7
| Molecular Weight: | 378.42 g./mol | Molecular Formula: | C₁₉H₂₆N₂O₆ |
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| EC Number: | MDL Number: | MFCD29920507 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it valuable in multi-step synthetic processes. Its chiral structure is crucial for producing enantiomerically pure substances, which is essential in drug development to ensure efficacy and reduce side effects. Additionally, it is employed in the preparation of proline derivatives, which are significant in designing enzyme inhibitors and receptor modulators.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | Ft24,241.74 |
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| 0.250 | 10-20 days | Ft40,726.13 |
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| 1.000 | 10-20 days | Ft83,876.43 |
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(2S,4S)-1-Benzyl 2-methyl 4-((tert-butoxycarbonyl)amino)pyrrolidine-1,2-dicarboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of peptidomimetics and other bioactive compounds. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions, making it valuable in multi-step synthetic processes. Its chiral structure is crucial for producing enantiomerically pure substances, which is essential in drug development to ensure efficacy and reduce side effects. Additionally, it is employed in the preparation of proline derivatives, which are significant in designing enzyme inhibitors and receptor modulators.
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