tert-Butyl 3-(((benzyloxy)carbonyl)amino)propanoate
≥95%
- Product Code: 50519
CAS:
18605-26-0
| Molecular Weight: | 279.33 g./mol | Molecular Formula: | C₁₅H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03837779 | |
| Melting Point: | Boiling Point: | 409.3°C at 760 mmHg | |
| Density: | 1.101g/cm3 | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily used in organic synthesis as a protected intermediate for the preparation of peptides and other bioactive molecules. The tert-butyl group acts as a protecting group for the carboxyl function, while the benzyloxycarbonyl (Cbz) group protects the amine function. This dual protection allows selective reactions to occur at other sites of the molecule without affecting these functional groups. It is particularly useful in the stepwise synthesis of complex organic molecules, where selective deprotection and further functionalization are required. The compound’s stability under various reaction conditions makes it a valuable tool in medicinal chemistry and pharmaceutical research for developing new drugs and therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft12,120.87 |
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| 1.000 | 10-20 days | Ft26,181.08 |
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| 5.000 | 10-20 days | Ft91,827.72 |
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| 10.000 | 10-20 days | Ft178,128.33 |
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tert-Butyl 3-(((benzyloxy)carbonyl)amino)propanoate
This compound is primarily used in organic synthesis as a protected intermediate for the preparation of peptides and other bioactive molecules. The tert-butyl group acts as a protecting group for the carboxyl function, while the benzyloxycarbonyl (Cbz) group protects the amine function. This dual protection allows selective reactions to occur at other sites of the molecule without affecting these functional groups. It is particularly useful in the stepwise synthesis of complex organic molecules, where selective deprotection and further functionalization are required. The compound’s stability under various reaction conditions makes it a valuable tool in medicinal chemistry and pharmaceutical research for developing new drugs and therapeutic agents.
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