1-(4-Azidopiperidin-1-yl)ethan-1-one
95%
- Product Code: 123820
CAS:
2098012-37-2
| Molecular Weight: | 168.2 g./mol | Molecular Formula: | C₇H₁₂N₄O |
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| Density: | Storage Condition: | room temperature |
Product Description:
1-(4-Azidopiperidin-1-yl)ethan-1-one is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. The azido group in its structure makes it valuable for click chemistry reactions, enabling efficient and selective coupling with alkynes to form triazole derivatives. This property is widely exploited in drug discovery and material science for creating complex molecular architectures. Additionally, it is employed in the preparation of piperidine-based compounds, which are commonly found in drugs targeting neurological disorders, inflammation, and other medical conditions. Its role in facilitating the construction of diverse chemical libraries underscores its importance in medicinal chemistry and chemical biology.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿20,313.00 |
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| 0.250 | 10-20 days | ฿52,830.00 |
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1-(4-Azidopiperidin-1-yl)ethan-1-one
1-(4-Azidopiperidin-1-yl)ethan-1-one is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of molecules with potential therapeutic applications. The azido group in its structure makes it valuable for click chemistry reactions, enabling efficient and selective coupling with alkynes to form triazole derivatives. This property is widely exploited in drug discovery and material science for creating complex molecular architectures. Additionally, it is employed in the preparation of piperidine-based compounds, which are commonly found in drugs targeting neurological disorders, inflammation, and other medical conditions. Its role in facilitating the construction of diverse chemical libraries underscores its importance in medicinal chemistry and chemical biology.
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