(S)-tert-Butyl 6-amino-2-((tert-butoxycarbonyl)amino)hexanoate hydrochloride
97%
- Product Code: 38588
CAS:
7750-45-0
| Molecular Weight: | 338.87 g./mol | Molecular Formula: | C₁₅H₃₁ClN₂O₄ |
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| EC Number: | MDL Number: | MFCD08275791 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a key intermediate in the production of biologically active molecules. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection are required. It is often employed in the development of pharmaceutical compounds, including drugs targeting neurological disorders and enzyme inhibitors. Additionally, its hydrochloride form enhances stability and solubility, facilitating its use in various chemical processes. The compound is also relevant in research focused on amino acid modification and the exploration of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,537.00 |
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| 1.000 | 10-20 days | ฿7,083.00 |
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(S)-tert-Butyl 6-amino-2-((tert-butoxycarbonyl)amino)hexanoate hydrochloride
This compound is primarily utilized in the synthesis of peptides and amino acid derivatives, serving as a key intermediate in the production of biologically active molecules. Its structure, featuring both amino and tert-butoxycarbonyl (Boc) protecting groups, makes it valuable in organic synthesis, particularly in peptide coupling reactions where selective protection and deprotection are required. It is often employed in the development of pharmaceutical compounds, including drugs targeting neurological disorders and enzyme inhibitors. Additionally, its hydrochloride form enhances stability and solubility, facilitating its use in various chemical processes. The compound is also relevant in research focused on amino acid modification and the exploration of novel therapeutic agents.
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