(2S,4R)-1-tert-butyl 2-methyl 4-(((benzyloxy)carbonyl)amino)pyrrolidine-1,2-dicarboxylate
95%
- Product Code: 82868
CAS:
130047-39-1
| Molecular Weight: | 378.42 g./mol | Molecular Formula: | C₁₉H₂₆N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18252794 | |
| Melting Point: | Boiling Point: | 504.5±50.0 °C(Predicted) | |
| Density: | 1.22±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
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. Its structure, featuring both tert-butyl and benzyloxycarbonyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. The compound is often employed in the construction of pyrrolidine-based frameworks, which are common in drug molecules targeting various diseases. Its chiral centers also enable its use in asymmetric synthesis, contributing to the production of enantiomerically pure substances.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,190.00 |
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| 0.250 | 10-20 days | ฿14,040.00 |
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| 1.000 | 10-20 days | ฿28,080.00 |
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(2S,4R)-1-tert-butyl 2-methyl 4-(((benzyloxy)carbonyl)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. Its structure, featuring both tert-butyl and benzyloxycarbonyl protecting groups, makes it valuable for selective deprotection strategies during multi-step synthetic processes. The compound is often employed in the construction of pyrrolidine-based frameworks, which are common in drug molecules targeting various diseases. Its chiral centers also enable its use in asymmetric synthesis, contributing to the production of enantiomerically pure substances.
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