tert-Butyl 2,5-dioxa-8-azaspiro[3.5]nonane-8-carboxylate

95%

Reagent Code: #75143
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CAS Number 1272412-69-7

science Other reagents with same CAS 1272412-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229 g/mol
Formula C₁₁H₁₉NO₄
badge Registry Numbers
MDL Number MFCD18782890
inventory_2 Storage & Handling
Storage 2-8°C, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis as a versatile building block, particularly in the development of complex molecules. Its spirocyclic structure makes it valuable for constructing constrained frameworks, which are often required in medicinal chemistry for drug discovery. The tert-butyl ester group provides stability and can be selectively removed under mild conditions, allowing for further functionalization. Additionally, the presence of nitrogen and oxygen atoms in the ring system enables its use in the synthesis of heterocycles, which are common motifs in pharmaceuticals and agrochemicals. Its application extends to the preparation of peptidomimetics and other biologically active compounds, where its rigid structure can mimic natural peptides and enhance binding affinity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿60,450.00
inventory 1g
10-20 days ฿182,220.00

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tert-Butyl 2,5-dioxa-8-azaspiro[3.5]nonane-8-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile building block, particularly in the development of complex molecules. Its spirocyclic structure makes it valuable for constructing constrained frameworks, which are often required in medicinal chemistry for drug discovery. The tert-butyl ester group provides stability and can be selectively removed under mild conditions, allowing for further functionalization. Additionally, the presence of nitrogen and oxygen atoms in the ring system enables its use in the synthesis of heterocycles, which are common motifs in pharmaceuticals and agrochemicals. Its application extends to the preparation of peptidomimetics and other biologically active compounds, where its rigid structure can mimic natural peptides and enhance binding affinity.
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