tert-Butyl 3-(2-ethoxy-2-oxoethyl)pyrrolidine-1-carboxylate

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Reagent Code: #65048
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CAS Number 664364-29-8

science Other reagents with same CAS 664364-29-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.33 g/mol
Formula C₁₃H₂₃NO₄
badge Registry Numbers
MDL Number MFCD11977331
thermostat Physical Properties
Boiling Point 321.4±15.0 °C at 760 mmHg
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 ester and pyrrolidine groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in the construction of nitrogen-containing heterocycles, which are common in drug molecules. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, enabling the controlled modification of specific functional groups. This compound is also used in research settings for the development of novel chemical entities and in medicinal chemistry studies to explore structure-activity relationships.

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Test Parameter Specification
Appearance Colorless to Light Yellow to Yellow-brown Liquid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿16,290.00
inventory 1g
10-20 days ฿4,716.00

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tert-Butyl 3-(2-ethoxy-2-oxoethyl)pyrrolidine-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 ester and pyrrolidine groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in the construction of nitrogen-containing heterocycles, which are common in drug molecules. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for select

This compound is primarily utilized in organic synthesis as an intermediate for the preparation of more complex molecules. Its structure, featuring both ester and pyrrolidine groups, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in the construction of nitrogen-containing heterocycles, which are common in drug molecules. Additionally, its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions in multi-step synthetic processes, enabling the controlled modification of specific functional groups. This compound is also used in research settings for the development of novel chemical entities and in medicinal chemistry studies to explore structure-activity relationships.

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