(2S,5R)-5-((Benzyloxy)amino)piperidine-2-carboxamide
97%
- Product Code: 70884
CAS:
1416134-49-0
| Molecular Weight: | 249.31 g./mol | Molecular Formula: | C₁₃H₁₉N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29472345 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its structure is often incorporated into the development of potential drug candidates for treating infectious diseases, neurological disorders, or inflammatory conditions. Researchers also explore its utility in creating peptidomimetics, which mimic the structure and function of peptides, aiding in the design of novel therapeutic agents. Additionally, its chiral centers make it valuable in stereoselective synthesis, enabling the production of enantiomerically pure compounds for enhanced drug efficacy and reduced side effects.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,026.00 |
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| 1.000 | 10-20 days | ฿2,619.00 |
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| 5.000 | 10-20 days | ฿9,072.00 |
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(2S,5R)-5-((Benzyloxy)amino)piperidine-2-carboxamide
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition or receptor modulation. Its structure is often incorporated into the development of potential drug candidates for treating infectious diseases, neurological disorders, or inflammatory conditions. Researchers also explore its utility in creating peptidomimetics, which mimic the structure and function of peptides, aiding in the design of novel therapeutic agents. Additionally, its chiral centers make it valuable in stereoselective synthesis, enabling the production of enantiomerically pure compounds for enhanced drug efficacy and reduced side effects.
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