Boc-3-(2-pyridyl)-L-alanine
98%
- Product Code: 104652
Alias:
Boc-3-(2-pyridyl)-L-alanine
CAS:
71239-85-5
| Molecular Weight: | 266.29 g./mol | Molecular Formula: | C₁₃H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191190 | |
| Melting Point: | Boiling Point: | 436.9ºC at 760 mmHg | |
| Density: | 1.2g/cm3 | Storage Condition: | room temperature |
Product Description:
Used primarily in peptide synthesis, Boc-3-(2-pyridyl)-L-alanine serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group safeguards the amino functionality during the synthesis process, preventing unwanted side reactions. This compound is particularly valuable in creating peptides with specific structural or functional properties, often utilized in research and pharmaceutical development. Its pyridyl group can introduce unique interactions, such as metal coordination or hydrogen bonding, enhancing the peptide's biological activity or stability. Additionally, it is employed in the study of enzyme-substrate interactions and the development of peptide-based drugs.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Crystal |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,610.00 |
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| 5.000 | 10-20 days | ฿4,930.00 |
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| 25.000 | 10-20 days | ฿19,940.00 |
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Boc-3-(2-pyridyl)-L-alanine
Used primarily in peptide synthesis, Boc-3-(2-pyridyl)-L-alanine serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group safeguards the amino functionality during the synthesis process, preventing unwanted side reactions. This compound is particularly valuable in creating peptides with specific structural or functional properties, often utilized in research and pharmaceutical development. Its pyridyl group can introduce unique interactions, such as metal coordination or hydrogen bonding, enhancing the peptide's biological activity or stability. Additionally, it is employed in the study of enzyme-substrate interactions and the development of peptide-based drugs.
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