tert-Butyl 9,9-difluoro-1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate
97%
- Product Code: 87909
CAS:
1373502-80-7
| Molecular Weight: | 290.306 g./mol | Molecular Formula: | C₁₃H₂₀F₂N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21602026 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a spirocyclic core and functional groups like the carboxylate ester, makes it a valuable building block for developing biologically active compounds. Researchers often employ it in the design and preparation of potential drug candidates, particularly those targeting neurological or inflammatory diseases. The difluoro and spirocyclic motifs are known to enhance metabolic stability and bioavailability, making it a useful scaffold in drug discovery. Additionally, its reactive sites allow for further chemical modifications, enabling the creation of diverse libraries of compounds for screening and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €1,256.76 |
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tert-Butyl 9,9-difluoro-1-oxo-2,7-diazaspiro[4.5]decane-7-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. Its structure, featuring a spirocyclic core and functional groups like the carboxylate ester, makes it a valuable building block for developing biologically active compounds. Researchers often employ it in the design and preparation of potential drug candidates, particularly those targeting neurological or inflammatory diseases. The difluoro and spirocyclic motifs are known to enhance metabolic stability and bioavailability, making it a useful scaffold in drug discovery. Additionally, its reactive sites allow for further chemical modifications, enabling the creation of diverse libraries of compounds for screening and optimization.
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