1-((1-Acetylpiperidin-2-yl)methyl)-1H-1,2,3-triazole-4-carbaldehyde
95%
- Product Code: 123750
CAS:
2098075-69-3
| Molecular Weight: | 236.27 g./mol | Molecular Formula: | C₁₁H₁₆N₄O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in medicinal chemistry and drug discovery due to its structural features, which make it a valuable intermediate for synthesizing biologically active molecules. The presence of the acetylpiperidinyl and triazole moieties allows it to interact with various biological targets, particularly enzymes and receptors, making it useful in the development of potential therapeutic agents. It is often employed in the design of compounds targeting neurological disorders, inflammation, and infectious diseases. Additionally, its aldehyde group provides a reactive site for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. Researchers also explore its use in click chemistry applications, where the triazole ring serves as a stable linker in bioconjugation processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿24,813.00 |
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| 0.250 | 10-20 days | ฿49,617.00 |
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1-((1-Acetylpiperidin-2-yl)methyl)-1H-1,2,3-triazole-4-carbaldehyde
This compound is primarily utilized in medicinal chemistry and drug discovery due to its structural features, which make it a valuable intermediate for synthesizing biologically active molecules. The presence of the acetylpiperidinyl and triazole moieties allows it to interact with various biological targets, particularly enzymes and receptors, making it useful in the development of potential therapeutic agents. It is often employed in the design of compounds targeting neurological disorders, inflammation, and infectious diseases. Additionally, its aldehyde group provides a reactive site for further chemical modifications, enabling the creation of diverse derivatives for structure-activity relationship studies. Researchers also explore its use in click chemistry applications, where the triazole ring serves as a stable linker in bioconjugation processes.
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