tert-butyl 6-((methylsulfonyl)oxy)-2-azaspiro[3.3]heptane-2-carboxylate
97%
- Product Code: 242833
CAS:
1239320-11-6
| Molecular Weight: | 291.36 g./mol | Molecular Formula: | C₁₂H₂₁NO₅S |
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| EC Number: | MDL Number: | MFCD29085851 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules, especially those targeting central nervous system disorders. The methylsulfonyloxy group acts as a leaving group, enabling nucleophilic substitution reactions to introduce various substituents. The tert-butoxycarbonyl (Boc) group protects the nitrogen, allowing selective deprotection and further derivatization in multi-step syntheses. Commonly employed in the development of kinase inhibitors and neuroactive agents.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | £85.85 |
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| 250mg | 10-20 days | £153.34 |
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| 1g | 10-20 days | £611.29 |
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| 5g | 10-20 days | £1,766.39 |
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tert-butyl 6-((methylsulfonyl)oxy)-2-azaspiro[3.3]heptane-2-carboxylate
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its spirocyclic structure and functional groups make it valuable for constructing complex molecules, especially those targeting central nervous system disorders. The methylsulfonyloxy group acts as a leaving group, enabling nucleophilic substitution reactions to introduce various substituents. The tert-butoxycarbonyl (Boc) group protects the nitrogen, allowing selective deprotection and further derivatization in multi-step syntheses. Commonly employed in the development of kinase inhibitors and neuroactive agents.
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