Methyl 3-((1,3-Dioxoisoindolin-2-Yl)Oxy)-2-Hydroxy-2-Methylpropanoate

97%

Reagent Code: #124608
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CAS Number 367520-87-4

science Other reagents with same CAS 367520-87-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.25 g/mol
Formula C₁₃H₁₃NO₆
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Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic applications. Its unique structure allows it to act as a key building block in the production of compounds with potential anti-inflammatory, anti-cancer, or antimicrobial properties. Additionally, it is employed in organic synthesis as a protective group for hydroxyl functionalities during complex multi-step reactions, ensuring selective transformations. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of novel drug candidates and bioactive molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,900.00
Methyl 3-((1,3-Dioxoisoindolin-2-Yl)Oxy)-2-Hydroxy-2-Methylpropanoate
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic applications. Its unique structure allows it to act as a key building block in the production of compounds with potential anti-inflammatory, anti-cancer, or antimicrobial properties. Additionally, it is employed in organic synthesis as a protective group for hydroxyl functionalities during complex multi-step reactions, ensuring s

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic applications. Its unique structure allows it to act as a key building block in the production of compounds with potential anti-inflammatory, anti-cancer, or antimicrobial properties. Additionally, it is employed in organic synthesis as a protective group for hydroxyl functionalities during complex multi-step reactions, ensuring selective transformations. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of novel drug candidates and bioactive molecules.

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