Ethyl 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoate

85%

Reagent Code: #69745
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CAS Number 88150-75-8

science Other reagents with same CAS 88150-75-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.31 g/mol
Formula C₁₆H₁₇NO₆
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. The presence of the 1,3-dioxoisoindolin moiety and the ester functional group makes it a versatile building block for constructing complex structures. It is often employed in the synthesis of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its reactivity allows for further modifications, enabling researchers to explore new chemical entities for drug discovery and development.

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Test Parameter Specification
Appearance Liquid or Solid
Purity 85-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿7,280.00
inventory 1g
10-20 days ฿20,380.00

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Ethyl 4-(2-(1,3-dioxoisoindolin-2-yl)ethoxy)-3-oxobutanoate
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. The presence of the 1,3-dioxoisoindolin moiety and the ester functional group makes it a versatile building block for constructing complex structures. It is often employed in the synthesis of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. A
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly those targeting therapeutic applications. The presence of the 1,3-dioxoisoindolin moiety and the ester functional group makes it a versatile building block for constructing complex structures. It is often employed in the synthesis of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its reactivity allows for further modifications, enabling researchers to explore new chemical entities for drug discovery and development.
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