tert-Butyl 7-(prop-2-yn-1-yl)-2,7-diazaspiro[3.5]nonane-2-carboxylate
97%
- Product Code: 67892
CAS:
2434850-33-4
| Molecular Weight: | 264.36 g./mol | Molecular Formula: | C₁₅H₂₄N₂O₂ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry as a key intermediate for the development of more complex molecules. Its structure, featuring a spirocyclic framework and a reactive alkyne group, makes it particularly valuable for click chemistry applications, where it can participate in copper-catalyzed azide-alkyne cycloaddition reactions. These reactions are widely employed in drug discovery, bioconjugation, and materials science for the efficient and selective formation of triazole linkages. Additionally, the tert-butyl ester group in the molecule provides a protective strategy for carboxylic acids, allowing for controlled deprotection during multi-step synthetic processes. Its versatility and reactivity make it a valuable building block in the design of novel pharmaceuticals and biologically active compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,011.00 |
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| 0.100 | 10-20 days | ฿11,214.00 |
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| 0.250 | 10-20 days | ฿19,053.00 |
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tert-Butyl 7-(prop-2-yn-1-yl)-2,7-diazaspiro[3.5]nonane-2-carboxylate
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry as a key intermediate for the development of more complex molecules. Its structure, featuring a spirocyclic framework and a reactive alkyne group, makes it particularly valuable for click chemistry applications, where it can participate in copper-catalyzed azide-alkyne cycloaddition reactions. These reactions are widely employed in drug discovery, bioconjugation, and materials science for the efficient and selective formation of triazole linkages. Additionally, the tert-butyl ester group in the molecule provides a protective strategy for carboxylic acids, allowing for controlled deprotection during multi-step synthetic processes. Its versatility and reactivity make it a valuable building block in the design of novel pharmaceuticals and biologically active compounds.
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