(R)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)propanoic acid
98%
- Product Code: 39548
Alias:
H-D-His(Trt)-OH
CAS:
199119-46-5
| Molecular Weight: | 397.47 g./mol | Molecular Formula: | C₂₅H₂₃N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 584.8±50.0 °C | |
| Density: | 1.19 | Storage Condition: | 2-8 °C |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and biochemistry as a key intermediate in the synthesis of complex molecules. It plays a significant role in the development of enzyme inhibitors and receptor modulators, particularly those targeting imidazole-related biological pathways. Its trityl-protected imidazole group makes it a valuable building block for peptide synthesis, enabling the creation of structurally diverse compounds with potential therapeutic applications. Researchers often employ it in the study of histidine-containing peptides and proteins, as well as in the design of novel drugs for treating conditions such as inflammation, cancer, and neurological disorders. Its chiral nature also allows for the exploration of stereospecific interactions in drug design, enhancing the precision of pharmacological agents.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $135.61 |
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| 5.000 | 10-20 days | $452.03 |
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(R)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)propanoic acid
This chemical is primarily utilized in the field of medicinal chemistry and biochemistry as a key intermediate in the synthesis of complex molecules. It plays a significant role in the development of enzyme inhibitors and receptor modulators, particularly those targeting imidazole-related biological pathways. Its trityl-protected imidazole group makes it a valuable building block for peptide synthesis, enabling the creation of structurally diverse compounds with potential therapeutic applications. Researchers often employ it in the study of histidine-containing peptides and proteins, as well as in the design of novel drugs for treating conditions such as inflammation, cancer, and neurological disorders. Its chiral nature also allows for the exploration of stereospecific interactions in drug design, enhancing the precision of pharmacological agents.
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