(R)-2-(((Benzyloxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid
95%
- Product Code: 37440
CAS:
214852-60-5
| Molecular Weight: | 352.3823 g./mol | Molecular Formula: | C₁₇H₂₄N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02094569 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of peptide synthesis as a protected amino acid derivative. Its structure, featuring both benzyloxycarbonyl (Cbz) and tert-butoxycarbonyl (Boc) protecting groups, allows for selective deprotection during the synthesis of complex peptides. The Cbz group can be removed via hydrogenolysis, while the Boc group is cleaved under acidic conditions, enabling sequential and controlled assembly of peptide chains. This makes it a valuable building block in the production of peptides for pharmaceutical research, particularly in developing drugs targeting specific biological pathways. Additionally, its chiral nature ensures the synthesis of enantiomerically pure peptides, which is crucial for maintaining biological activity and efficacy in therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $150.41 |
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(R)-2-(((Benzyloxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid
This compound is primarily utilized in the field of peptide synthesis as a protected amino acid derivative. Its structure, featuring both benzyloxycarbonyl (Cbz) and tert-butoxycarbonyl (Boc) protecting groups, allows for selective deprotection during the synthesis of complex peptides. The Cbz group can be removed via hydrogenolysis, while the Boc group is cleaved under acidic conditions, enabling sequential and controlled assembly of peptide chains. This makes it a valuable building block in the production of peptides for pharmaceutical research, particularly in developing drugs targeting specific biological pathways. Additionally, its chiral nature ensures the synthesis of enantiomerically pure peptides, which is crucial for maintaining biological activity and efficacy in therapeutic applications.
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