Boc-3-(3-Pyridyl)-Alanine
99%
- Product Code: 104750
Alias:
BOC-L-3-(3-pyridyl)-alanine; Boc-3-(3-pyridyl)-L-alanine, N-tert-butoxycarbonyl-3-pyridyl-L-alanine sour
CAS:
117142-26-4
| Molecular Weight: | 266.29 g./mol | Molecular Formula: | C₁₃H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00079681 | |
| Melting Point: | 136-142 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative, enabling the controlled construction of peptide chains. It is particularly valuable in research and development of biologically active peptides, where the Boc (tert-butoxycarbonyl) group provides temporary protection for the amine functionality during synthesis. This allows for selective reactions at other sites of the molecule, ensuring precise peptide assembly. Its pyridyl side chain can also contribute to interactions in peptide-protein binding studies, making it useful in drug discovery and biochemical research.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 136-142 |
| Purity (HPLC) | 99-100 |
| Specific Rotation [A]20/DC = 1%, Ethanol | 14.5-16.5 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,755.00 |
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| 5.000 | 10-20 days | ฿6,300.00 |
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| 25.000 | 10-20 days | ฿31,113.00 |
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Boc-3-(3-Pyridyl)-Alanine
Used primarily in peptide synthesis, this compound serves as a protected amino acid derivative, enabling the controlled construction of peptide chains. It is particularly valuable in research and development of biologically active peptides, where the Boc (tert-butoxycarbonyl) group provides temporary protection for the amine functionality during synthesis. This allows for selective reactions at other sites of the molecule, ensuring precise peptide assembly. Its pyridyl side chain can also contribute to interactions in peptide-protein binding studies, making it useful in drug discovery and biochemical research.
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