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Structure of 18668-74-1
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3-(2-Bromoethoxy)prop-1-yne features a reactive terminal alkyne paired with a bromoethoxy handle, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC). This bifunctional architecture supports rapid conjugation in bioorthogonal labeling and polymer functionalization. The molecule exhibits high stability under standard bench conditions and facilitates site-specific modification in complex media.
3-(2-Bromoethoxy)prop-1-yne serves as a versatile building block for copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling efficient access to triazole-containing scaffolds. The terminal alkyne functionality facilitates reliable click chemistry under mild conditions, while the pendant bromoethoxy group provides orthogonal reactivity for further functionalization via nucleophilic substitution. Its bench-stable nature and compatibility with diverse reaction environments make 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: