(S)-Tert-butyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate
98%
- Product Code: 57156
CAS:
63628-63-7
| Molecular Weight: | 336.43 g./mol | Molecular Formula: | C₁₈H₂₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22581338 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, protected from light, stored under inert gas |
Product Description:
This compound is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The tert-butyl group acts as a protective moiety for the carboxyl group, while the benzyloxycarbonyl (Cbz) group protects the amino group. This dual protection allows for selective deprotection during the synthesis of complex peptides, ensuring the desired sequence is achieved without unwanted side reactions. It is particularly valuable in the production of custom peptides for pharmaceutical research, enabling the development of new drugs and therapeutic agents. Additionally, its chiral nature makes it suitable for synthesizing enantiomerically pure compounds, which are crucial in medicinal chemistry for targeting specific biological pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,825.00 |
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| 0.250 | 10-20 days | ฿5,742.00 |
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| 1.000 | 10-20 days | ฿14,364.00 |
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(S)-Tert-butyl 2-amino-6-(((benzyloxy)carbonyl)amino)hexanoate
This compound is primarily used in peptide synthesis, where it serves as a protected amino acid derivative. The tert-butyl group acts as a protective moiety for the carboxyl group, while the benzyloxycarbonyl (Cbz) group protects the amino group. This dual protection allows for selective deprotection during the synthesis of complex peptides, ensuring the desired sequence is achieved without unwanted side reactions. It is particularly valuable in the production of custom peptides for pharmaceutical research, enabling the development of new drugs and therapeutic agents. Additionally, its chiral nature makes it suitable for synthesizing enantiomerically pure compounds, which are crucial in medicinal chemistry for targeting specific biological pathways.
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