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Structure of 1421503-53-8
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tert-Butyl 2-iodo-6,7-dihydro-1H-imidazo[4,5-c]pyridine-5(4H)-carboxylate features a bench-stable iodinated imidazopyridine core with enhanced solubility from the tert-butyl ester. This building block integrates readily into palladium-catalyzed cross-coupling reactions, enabling efficient access to complex heterocyclic scaffolds in medicinal chemistry and materials science applications.
tert-Butyl 2-iodo-6,7-dihydro-1H-imidazo[4,5-c]pyridine-5(4H)-carboxylate serves as a versatile building block for the synthesis of imidazopyridine-based scaffolds. The iodide functionality enables efficient Pd-catalyzed cross-coupling reactions, while the protected carboxylate group offers stability and compatibility with diverse reaction conditions. Its bench-stable nature and functional group tolerance facilitate straightforward incorporation into complex molecular architectures relevant to medicinal chemistry and agrochemical research.
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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: