tert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate

97%

Reagent Code: #238291
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CAS Number 154348-08-0

science Other reagents with same CAS 154348-08-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.314 g/mol
Formula C₁₃H₂₁NO₄
badge Registry Numbers
MDL Number MFCD13184732
thermostat Physical Properties
Boiling Point 399.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with central nervous system activity. Its spirocyclic structure and protected amine functionality make it valuable in medicinal chemistry for constructing complex heterocycles. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl carbamate (Boc) group allows for selective deprotection under mild conditions, enabling stepwise assembly of multi-step synthetic pathways. Also utilized in the design of prodrugs and in peptide mimetics due to its stability and conformational rigidity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,650.00
inventory 500mg
10-20 days ฿17,090.00

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tert-butyl 1-oxo-2-oxa-8-azaspiro[4.5]decane-8-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with central nervous system activity. Its spirocyclic structure and protected amine functionality make it valuable in medicinal chemistry for constructing complex heterocycles. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl carbamate (Boc) group allows for selective deprotect

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with central nervous system activity. Its spirocyclic structure and protected amine functionality make it valuable in medicinal chemistry for constructing complex heterocycles. Commonly employed in the preparation of enzyme inhibitors and receptor modulators, especially in research targeting neurological disorders. The tert-butyl carbamate (Boc) group allows for selective deprotection under mild conditions, enabling stepwise assembly of multi-step synthetic pathways. Also utilized in the design of prodrugs and in peptide mimetics due to its stability and conformational rigidity.

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