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Structure of 7223-50-9
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This isoindoline-1,3-dione derivative features a propargyl group at the 2-position, enabling efficient copper-catalyzed azide-alkyne cycloaddition. The electron-deficient dione core facilitates conjugate addition reactions, while the alkyne handle offers orthogonal reactivity for bioconjugation and materials functionalization under mild conditions.
2-(Prop-2-yn-1-yl)isoindoline-1,3-dione serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized isoindolinone scaffolds. The terminal alkyne group facilitates CuAAC and other transition-metal-catalyzed coupling reactions, while the phthalimide moiety provides excellent stability and orthogonal reactivity. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for modular synthesis workflows in medicinal chemistry and materials science.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: