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Structure of 17720-64-8
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1,3-Dioxoisoindolin-2-yl acetate features a stabilized isoindolinone core with a strategically positioned acetyl group, enhancing reactivity in electrophilic transformations. This bench-stable derivative integrates readily into synthetic sequences requiring controlled carbonyl functionality, particularly in the development of bioactive heterocycles and advanced intermediates for medicinal chemistry applications.
1,3-Dioxoisoindolin-2-yl acetate serves as a versatile building block for the synthesis of isoindolinone-based scaffolds prevalent in medicinal chemistry. Its acetylated dione functionality enables selective deprotection and downstream functionalization, while maintaining bench stability and compatibility with common coupling reactions. The molecule facilitates efficient access to heterocyclic frameworks through controlled cyclization and oxidation protocols, supporting scalable synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS02,GHS07
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Signal Word : Danger
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UN#: 1325
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Class : 4.1
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Packing Group : Ⅱ
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Hazard Statements : H228-H315-H319
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Precautionary Statements : P210-P240-P241-P264-P280-P302+P352-P362+P364-P370+P378
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Lot numbers can be found on the outside label of a product: