(S)-1-tert-butyl 2-ethyl 4,4-dimethyl-5-oxopyrrolidine-1,2-dicarboxylate

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Reagent Code: #82993
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CAS Number 158392-80-4

science Other reagents with same CAS 158392-80-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₁₄H₂₃NO₅
badge Registry Numbers
MDL Number MFCD17926379
thermostat Physical Properties
Boiling Point 383.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.114±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both ester and ketone functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of chiral compounds. The tert-butyl and ethyl ester groups provide steric protection and selective reactivity, which is beneficial in multi-step synthetic processes. It is often employed in the construction of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Additionally, its chiral nature allows for the creation of enantiomerically pure substances, which are critical in the production of drugs with specific stereochemical requirements.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿23,355.00
inventory 100mg
10-20 days ฿5,094.00
inventory 250mg
10-20 days ฿8,658.00

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(S)-1-tert-butyl 2-ethyl 4,4-dimethyl-5-oxopyrrolidine-1,2-dicarboxylate
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This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both ester and ketone functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of chiral compounds. The tert-butyl and ethyl ester groups provide steric protection and selective reactivity, which is beneficial in multi-step synthetic processes. It is often employed in the construction of pyrrolidine-based framework

This compound is primarily used in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both ester and ketone functional groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of chiral compounds. The tert-butyl and ethyl ester groups provide steric protection and selective reactivity, which is beneficial in multi-step synthetic processes. It is often employed in the construction of pyrrolidine-based frameworks, which are common in bioactive molecules and drug candidates. Additionally, its chiral nature allows for the creation of enantiomerically pure substances, which are critical in the production of drugs with specific stereochemical requirements.

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