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Structure of 164118-56-3
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This alkyne features a 2-iodoethoxy substituent, enabling efficient copper-catalyzed coupling reactions. The terminal alkyne functionality integrates readily into complex molecular architectures, while the iodoether group supports orthogonal transformations. Stable under standard conditions, this reagent streamlines access to functionalized alkynyl motifs in synthetic workflows.
3-(2-Iodoethoxy)prop-1-yne serves as a versatile bifunctional building block for copper-catalyzed azide-alkyne cycloaddition (CuAAC) and cross-coupling reactions. The terminal alkyne enables efficient triazole formation, while the pendant iodide supports palladium-catalyzed coupling with arylboranes or amines. Its bench-stable nature and compatibility with diverse functional groups facilitate streamlined synthesis of complex scaffolds 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: