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Structure of 65881-41-6
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N-(Prop-2-yn-1-yl)acetamide features a terminal alkyne group flanked by a polar amide functionality, enabling efficient copper-catalyzed azide-alkyne cycloaddition. This bifunctional scaffold integrates readily into bioconjugation workflows and small-molecule libraries, offering high chemoselectivity and compatibility under standard bench conditions.
N-(Prop-2-yn-1-yl)acetamide serves as a versatile synthetic building block, enabling efficient access to functionalized alkynes via straightforward derivatization. The propargylic amide functionality exhibits excellent bench stability and compatibility with standard coupling protocols. It functions effectively in copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating rapid construction of triazole-linked scaffolds commonly employed in medicinal chemistry and materials science. Its moderate reactivity profile allows for selective transformations under mild conditions, supporting purification by standard chromatographic techniques.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: