(R)-N-Boc-(2-Pyridyl)alanine
99%
- Product Code: 104683
Alias:
BOC-D-3-(2-pyridyl)-alanine
CAS:
98266-32-1
| Molecular Weight: | 266.3 g./mol | Molecular Formula: | C₁₃H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191190 | |
| Melting Point: | 145-152 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This compound is widely used in the field of peptide synthesis, particularly as a building block for creating complex peptide structures. Its chiral nature makes it valuable in the development of enantiomerically pure peptides, which are essential in pharmaceutical research for designing drugs with specific biological activities. The Boc (tert-butoxycarbonyl) protecting group ensures selective reactions during peptide chain assembly, allowing for precise control over the synthesis process. Additionally, the pyridyl group in its structure can enhance the binding affinity of peptides to certain biological targets, making it useful in the design of enzyme inhibitors or receptor ligands. Its application extends to medicinal chemistry, where it aids in the development of potential therapeutic agents targeting various diseases.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 99-100 |
| Specific Rotation [A]20/D(C=1, In Meoh) | 15 Degree Celsius - 20 Degree Celsius |
| Melting Point | 140-145 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $52.81 |
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| 5.000 | 10-20 days | $207.38 |
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(R)-N-Boc-(2-Pyridyl)alanine
This compound is widely used in the field of peptide synthesis, particularly as a building block for creating complex peptide structures. Its chiral nature makes it valuable in the development of enantiomerically pure peptides, which are essential in pharmaceutical research for designing drugs with specific biological activities. The Boc (tert-butoxycarbonyl) protecting group ensures selective reactions during peptide chain assembly, allowing for precise control over the synthesis process. Additionally, the pyridyl group in its structure can enhance the binding affinity of peptides to certain biological targets, making it useful in the design of enzyme inhibitors or receptor ligands. Its application extends to medicinal chemistry, where it aids in the development of potential therapeutic agents targeting various diseases.
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