N-(tert-Butoxycarbonyl)-L-leucine N′-methoxy-N′-methylamide
98%
- Product Code: 57999
CAS:
87694-50-6
| Molecular Weight: | 274.36 g./mol | Molecular Formula: | C₁₃H₂₆N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151875 | |
| Melting Point: | Boiling Point: | 235 °C(lit.) | |
| Density: | 1.46 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in the preparation of complex peptides and proteins, ensuring specific amino acids are incorporated correctly during synthesis. The tert-butoxycarbonyl (Boc) group protects the amine functionality, preventing unwanted reactions, while the methoxy-methylamide moiety enhances solubility and facilitates coupling reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS) and other organic synthesis applications where controlled and selective reactions are essential. Its stability and ease of deprotection make it a reliable choice for researchers in medicinal chemistry and biochemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $42.04 |
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| 5.000 | 10-20 days | $141.94 |
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N-(tert-Butoxycarbonyl)-L-leucine N′-methoxy-N′-methylamide
This chemical is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block in the preparation of complex peptides and proteins, ensuring specific amino acids are incorporated correctly during synthesis. The tert-butoxycarbonyl (Boc) group protects the amine functionality, preventing unwanted reactions, while the methoxy-methylamide moiety enhances solubility and facilitates coupling reactions. It is particularly valuable in solid-phase peptide synthesis (SPPS) and other organic synthesis applications where controlled and selective reactions are essential. Its stability and ease of deprotection make it a reliable choice for researchers in medicinal chemistry and biochemistry.
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