1,8-Diazaspiro[4.5]decane-8-carboxylicacid tert-butyl ester
95%
- Product Code: 74901
CAS:
937729-06-1
| Molecular Weight: | 240.34 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11501187 | |
| Melting Point: | Boiling Point: | 337.0±35.0℃ at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, inert gas, protected from light |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its spirocyclic structure makes it particularly valuable in the development of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is often employed in the synthesis of complex organic molecules due to its stability and reactivity, which can be tailored for specific chemical transformations. Its tert-butyl ester group provides a protective function during synthetic processes, allowing for selective reactions to occur without interference. This compound is also explored in medicinal chemistry research for designing novel drug candidates with improved pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft23,756.91 |
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| 0.250 | 10-20 days | Ft41,889.73 |
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| 1.000 | 10-20 days | Ft107,730.31 |
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1,8-Diazaspiro[4.5]decane-8-carboxylicacid tert-butyl ester
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and bioactive molecules. Its spirocyclic structure makes it particularly valuable in the development of compounds with potential therapeutic applications, such as enzyme inhibitors or receptor modulators. Additionally, it is often employed in the synthesis of complex organic molecules due to its stability and reactivity, which can be tailored for specific chemical transformations. Its tert-butyl ester group provides a protective function during synthetic processes, allowing for selective reactions to occur without interference. This compound is also explored in medicinal chemistry research for designing novel drug candidates with improved pharmacokinetic properties.
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