1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-1,2,3-triazole-4-carboxylic acid
95%
- Product Code: 39096
CAS:
1119452-31-1
| Molecular Weight: | 296.3223 g./mol | Molecular Formula: | C₁₃H₂₀N₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12027299 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperidine ring and a triazole moiety, makes it a valuable building block for the development of pharmaceuticals, particularly in the design of protease inhibitors and other enzyme-targeting drugs. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the creation of complex drug candidates. Additionally, its carboxylic acid functionality provides a versatile handle for further chemical modifications, such as amide bond formation, which is crucial in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $243.19 |
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1-(1-(tert-Butoxycarbonyl)piperidin-4-yl)-1H-1,2,3-triazole-4-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring both a piperidine ring and a triazole moiety, makes it a valuable building block for the development of pharmaceuticals, particularly in the design of protease inhibitors and other enzyme-targeting drugs. The tert-butoxycarbonyl (Boc) protecting group allows for selective deprotection during multi-step synthetic processes, enabling the creation of complex drug candidates. Additionally, its carboxylic acid functionality provides a versatile handle for further chemical modifications, such as amide bond formation, which is crucial in drug discovery and development.
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