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Structure of 30413-58-2
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2-Ethynyl-6-methylpyridine features a conjugated alkyne group flanked by an electron-rich pyridine ring and a methyl substituent, enabling efficient copper-catalyzed coupling reactions. This bench-stable, moisture-tolerant building block integrates readily into complex molecular architectures via click chemistry protocols.
2-Ethynyl-6-methylpyridine serves as a versatile building block in transition-metal-catalyzed coupling reactions, enabling efficient access to substituted pyridine scaffolds. Its terminal alkyne functionality exhibits high compatibility with Sonogashira, Glaser, and click chemistry protocols, while the methyl group enhances electronic modulation and metabolic stability. Bench-stable and readily purified by column chromatography, it functions effectively in both small-molecule synthesis and medicinal chemistry campaigns.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: