Boc-3-(2-pyridyl)-L-alanine
98%
- Product Code: 124909
CAS:
65813-55-0
| Molecular Weight: | 220.2643 g./mol | Molecular Formula: | C₁₃H₁₆O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08275584 | |
| Melting Point: | Boiling Point: | 377.952℃ at 760 mmHg | |
| Density: | 1.107g/ml | Storage Condition: | 2-8℃, dry |
Product Description:
This compound is primarily used in peptide synthesis as a protected form of L-alanine. The Boc (tert-butoxycarbonyl) group safeguards the amino group during the peptide chain assembly, while the pyridyl side chain can participate in coordination chemistry or act as a ligand in metal complexes. It is particularly useful in designing peptides with specific structural or functional properties, such as those intended for biochemical studies or drug development. Additionally, the pyridyl moiety can enhance the solubility of peptides in aqueous solutions, making it valuable in creating biologically active compounds. Its application extends to research involving enzyme inhibitors, receptor ligands, and other bioactive molecules.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Off-White To Light Yellow Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | €149.85 |
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| 0.005 | 10-20 days | €358.80 |
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| 0.025 | 10-20 days | €1,253.67 |
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Boc-3-(2-pyridyl)-L-alanine
This compound is primarily used in peptide synthesis as a protected form of L-alanine. The Boc (tert-butoxycarbonyl) group safeguards the amino group during the peptide chain assembly, while the pyridyl side chain can participate in coordination chemistry or act as a ligand in metal complexes. It is particularly useful in designing peptides with specific structural or functional properties, such as those intended for biochemical studies or drug development. Additionally, the pyridyl moiety can enhance the solubility of peptides in aqueous solutions, making it valuable in creating biologically active compounds. Its application extends to research involving enzyme inhibitors, receptor ligands, and other bioactive molecules.
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