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Structure of 73746-43-7
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2-Iodo-5-methyl-1H-imidazole delivers a reactive iodine handle paired with a methyl-substituted imidazole core, enabling efficient coupling in cross-coupling and bioconjugation workflows. The electron-rich heterocycle enhances stability under standard conditions, while the para-iodo functionality facilitates selective transformations. This bench-stable reagent integrates readily into complex molecular architectures.
2-Iodo-5-methyl-1H-imidazole serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions with high efficiency. The iodide group facilitates reliable C–C and C–heteroatom bond formation under standard conditions, while the methyl-substituted imidazole core provides stability and orthogonal reactivity. This compound functions effectively in the construction of biologically relevant scaffolds and is well-suited for iterative synthesis workflows requiring bench-stable, selectively reactive intermediates.
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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: