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Structure of 1849257-78-8
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2-Ethynylpyridin-3-amine features a reactive alkyne group conjugated to a pyridyl amine, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) for bioconjugation and materials synthesis. This bench-stable compound integrates readily into functional architectures via click chemistry, offering high selectivity and yield under mild conditions.
2-Ethynylpyridin-3-amine serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted heterocycles via copper-catalyzed coupling reactions. Its terminal alkyne and primary amine functionalities offer orthogonal reactivity for click chemistry, Suzuki-Miyaura couplings, and amide bond formation. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative 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: