tert-butyl 3'-bromo-5',7'-dihydrospiro[[1,4]oxazepane-6,6'-pyrrolo[1,2-a]imidazole]-4-carboxylate
95%
- Product Code: 124128
CAS:
2177263-33-9
| Molecular Weight: | 372.26 g./mol | Molecular Formula: | C₁₅H₂₂BrN₃O₃ |
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| Density: | Storage Condition: | room temperature |
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 unique structure, featuring a spirocyclic framework and a bromo substituent, makes it a valuable building block for the development of potential drug candidates. Researchers often employ it in the design and synthesis of compounds targeting various therapeutic areas, such as central nervous system disorders, inflammation, and oncology. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, enhancing its versatility in synthetic pathways. The compound’s structural complexity also makes it a subject of interest in the study of novel heterocyclic chemistry and reaction mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $540.05 |
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tert-butyl 3'-bromo-5',7'-dihydrospiro[[1,4]oxazepane-6,6'-pyrrolo[1,2-a]imidazole]-4-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its unique structure, featuring a spirocyclic framework and a bromo substituent, makes it a valuable building block for the development of potential drug candidates. Researchers often employ it in the design and synthesis of compounds targeting various therapeutic areas, such as central nervous system disorders, inflammation, and oncology. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, enhancing its versatility in synthetic pathways. The compound’s structural complexity also makes it a subject of interest in the study of novel heterocyclic chemistry and reaction mechanisms.
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