Tert-butyl3-bromo-1-oxa-8-azaspiro[4.5]decane-8-carboxylate

97%

Reagent Code: #238280
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CAS Number 898157-46-5

science Other reagents with same CAS 898157-46-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.22 g/mol
Formula C₁₃H₂₂BrNO₃
badge Registry Numbers
MDL Number MFCD08098461
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of nitrogen-containing heterocyclic compounds. Its spirocyclic structure and functional groups make it valuable for constructing complex scaffolds in drug discovery. Commonly employed in coupling reactions to introduce the spiro moiety into target molecules, especially in central nervous system agents and enzyme inhibitors. The tert-butyl carbamate (Boc) group allows for protection of the amine during multi-step syntheses, enabling selective reactivity. Also utilized in the development of novel receptor ligands due to its conformational rigidity and stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,850.00
inventory 500mg
10-20 days ฿34,650.00

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Tert-butyl3-bromo-1-oxa-8-azaspiro[4.5]decane-8-carboxylate
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Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of nitrogen-containing heterocyclic compounds. Its spirocyclic structure and functional groups make it valuable for constructing complex scaffolds in drug discovery. Commonly employed in coupling reactions to introduce the spiro moiety into target molecules, especially in central nervous system agents and enzyme inhibitors. The tert-butyl carbamate (Boc) group allows for protection of th

Used in pharmaceutical synthesis as an intermediate for developing bioactive molecules, particularly in the production of nitrogen-containing heterocyclic compounds. Its spirocyclic structure and functional groups make it valuable for constructing complex scaffolds in drug discovery. Commonly employed in coupling reactions to introduce the spiro moiety into target molecules, especially in central nervous system agents and enzyme inhibitors. The tert-butyl carbamate (Boc) group allows for protection of the amine during multi-step syntheses, enabling selective reactivity. Also utilized in the development of novel receptor ligands due to its conformational rigidity and stability.

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