(S)-5-Amino-2-((S)-2-(((benzyloxy)carbonyl)amino)propanamido)-5-oxopentanoic acid
97%
- Product Code: 96148
CAS:
21467-17-4
| Molecular Weight: | 351.35 g./mol | Molecular Formula: | C₁₆H₂₁N₃O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00155524 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in peptide synthesis, where it serves as a building block for creating complex peptide structures. Its specific stereochemistry makes it valuable for synthesizing peptides with defined configurations, which is crucial in developing bioactive peptides and pharmaceutical agents. The benzyloxycarbonyl (Cbz) protecting group in the molecule ensures selective deprotection during peptide chain assembly, allowing for controlled and efficient synthesis. Additionally, it finds application in research focused on enzyme inhibitors and receptor ligands, particularly in studies targeting diseases where peptide interactions play a key role. Its stability and reactivity make it a preferred choice in organic and medicinal chemistry laboratories.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿801.00 |
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| 25.000 | 10-20 days | ฿2,700.00 |
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(S)-5-Amino-2-((S)-2-(((benzyloxy)carbonyl)amino)propanamido)-5-oxopentanoic acid
This compound is primarily utilized in peptide synthesis, where it serves as a building block for creating complex peptide structures. Its specific stereochemistry makes it valuable for synthesizing peptides with defined configurations, which is crucial in developing bioactive peptides and pharmaceutical agents. The benzyloxycarbonyl (Cbz) protecting group in the molecule ensures selective deprotection during peptide chain assembly, allowing for controlled and efficient synthesis. Additionally, it finds application in research focused on enzyme inhibitors and receptor ligands, particularly in studies targeting diseases where peptide interactions play a key role. Its stability and reactivity make it a preferred choice in organic and medicinal chemistry laboratories.
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