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Structure of 123523-58-0
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N-(Prop-2-yn-1-yl)acrylamide features a reactive alkyne handle and electron-deficient acrylamide moiety, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC). This bifunctional architecture supports site-specific conjugation in bioorthogonal labeling workflows.
N-(Prop-2-yn-1-yl)acrylamide serves as a versatile bifunctional building block in synthetic chemistry, combining a terminal alkyne and an acrylamide moiety for orthogonal reactivity. It enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) and Michael addition reactions, facilitating the construction of complex heterocycles and conjugated systems. The molecule exhibits excellent bench stability and is compatible with a range of functional groups, making it well-suited for modular synthesis in medicinal chemistry and materials science applications.
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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: