tert-Butyl 3-(3-ethoxy-3-oxopropanoyl)azetidine-1-carboxylate

≥95%

Reagent Code: #83514
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CAS Number 1025029-60-0

science Other reagents with same CAS 1025029-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.31 g/mol
Formula C₁₃H₂₁NO₅
badge Registry Numbers
MDL Number MFCD11974391
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both azetidine and ester functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds. The tert-butyl group provides steric protection, allowing selective reactions at other sites of the molecule. It is often employed in the construction of nitrogen-containing heterocycles, which are common motifs in drug discovery. Additionally, the ethoxy group can be hydrolyzed or transformed, enabling further functionalization for tailored applications in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,550.00

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tert-Butyl 3-(3-ethoxy-3-oxopropanoyl)azetidine-1-carboxylate
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This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both azetidine and ester functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds. The tert-butyl group provides steric protection, allowing selective reactions at other sites of the molecule. It is often employed in the construction of nitrogen-containing heterocycles, which are common m

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both azetidine and ester functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds. The tert-butyl group provides steric protection, allowing selective reactions at other sites of the molecule. It is often employed in the construction of nitrogen-containing heterocycles, which are common motifs in drug discovery. Additionally, the ethoxy group can be hydrolyzed or transformed, enabling further functionalization for tailored applications in medicinal chemistry.

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