1-tert-Butyl 3-ethyl 3-methyl-4-oxopyrrolidine-1,3-dicarboxylate

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Reagent Code: #76220
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CAS Number 897043-85-5

science Other reagents with same CAS 897043-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.31 g/mol
Formula C₁₃H₂₁NO₅
badge Registry Numbers
MDL Number MFCD17012785
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. The compound is often employed in the preparation of pyrrolidine derivatives, which are essential in the creation of various biologically active compounds. Additionally, its reactive carbonyl group allows for further functionalization, enabling chemists to tailor the molecule for specific applications in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿7,092.00
inventory 250mg
10-20 days ฿2,718.00

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1-tert-Butyl 3-ethyl 3-methyl-4-oxopyrrolidine-1,3-dicarboxylate
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This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. The compound is often employed in the preparation of pyrrolidine derivatives, which are essential in the creation of various biologically active compounds. Additionally, its reactive carbonyl group allows for further functional

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both tert-butyl and ethyl ester groups, makes it a versatile building block in the synthesis of pharmaceuticals and agrochemicals. The compound is often employed in the preparation of pyrrolidine derivatives, which are essential in the creation of various biologically active compounds. Additionally, its reactive carbonyl group allows for further functionalization, enabling chemists to tailor the molecule for specific applications in drug discovery and material science.

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