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Structure of 69022-70-4
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3-(Prop-2-yn-1-yloxy)pyridine features a reactive alkyne handle tethered to a pyridine heterocycle, enabling efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC). The propargylic ether linkage ensures stability under standard conditions while facilitating conjugation with azide-functionalized biomolecules or materials. This compound serves as a robust scaffold for bioconjugation and click chemistry applications.
3-(Prop-2-yn-1-yloxy)pyridine serves as a versatile building block in synthetic organic chemistry, enabling efficient CuAAC (copper-catalyzed azide-alkyne cycloaddition) reactions due to its terminal alkyne functionality. The pyridine moiety provides a stable heteroaromatic scaffold with moderate basicity and favorable electronic properties for further functionalization. This compound exhibits excellent bench stability, facilitates straightforward purification via chromatography, and demonstrates broad compatibility with common protecting groups and reaction conditions in medicinal chemistry and materials synthesis workflows.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: