(R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate
≥95%
- Product Code: 82964
CAS:
1093198-33-4
| Molecular Weight: | 246.30 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28991774 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of complex organic compounds, particularly in pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during peptide synthesis, allowing for precise control over the assembly of amino acid sequences. Its chiral nature makes it valuable in the development of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in the study of enzyme mechanisms and protein structures, aiding in the understanding of biochemical processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿20,250.00 |
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(R)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate
This compound is primarily utilized in the synthesis of peptides and other biologically active molecules. It serves as a key intermediate in the production of complex organic compounds, particularly in pharmaceutical research. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during peptide synthesis, allowing for precise control over the assembly of amino acid sequences. Its chiral nature makes it valuable in the development of enantiomerically pure drugs, enhancing their efficacy and reducing potential side effects. Additionally, it is employed in the study of enzyme mechanisms and protein structures, aiding in the understanding of biochemical processes.
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