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Structure of 1631179-23-1
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This 1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl 2-methylpropanoate features a sterically hindered isobutyrate ester linked to a reactive isoindolinone core. The electron-deficient carbonyl system enhances its utility in nucleophilic displacement reactions and cycloadditions. Bench-stable under standard conditions, it serves as a key building block for heterocyclic synthesis and materials chemistry applications.
1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl 2-methylpropanoate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to isoindolinone scaffolds through standard deprotection and cyclization protocols. Its robust bench stability and compatibility with diverse functional groups facilitate straightforward purification and integration into multi-step syntheses. The molecule functions effectively in coupling reactions and provides a reliable route to medicinally relevant heterocycles.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: