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Structure of 2154356-63-3
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This isoindoline-1,3-dione derivative features a reactive ethynyl group enabling efficient coupling in click chemistry applications. The piperidinone moiety imparts stability and enhances solubility, while the electron-deficient core facilitates conjugate addition reactions. Designed for modular synthesis in bioconjugation and medicinal chemistry workflows.
2-(2,6-Dioxopiperidin-3-yl)-5-ethynylisoindoline-1,3-dione serves as a versatile building block for the construction of complex heterocyclic scaffolds. The terminal alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating rapid access to triazole-linked architectures. Its isoindoline-1,3-dione core exhibits excellent bench stability and compatibility with diverse functional groups, making it well-suited for modular synthesis in medicinal chemistry and materials science applications.
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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+P364-P405-P501
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Lot numbers can be found on the outside label of a product: