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Structure of 1788043-93-5
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Methyl 3-iodo-1H-indole-7-carboxylate features a sterically accessible indole core functionalized at the 3-position with a reactive iodide and at the 7-position with a methyl ester. This combination enables direct cross-coupling transformations while maintaining stability under standard bench conditions, facilitating efficient access to complex indole architectures in medicinal chemistry and materials synthesis.
Methyl 3-iodo-1H-indole-7-carboxylate serves as a versatile building block for late-stage functionalization in medicinal chemistry and heterocyclic synthesis. The iodine substituent enables palladium-catalyzed cross-coupling reactions, while the ester group offers compatibility with standard deprotection and derivatization protocols. Bench-stable and readily purified by flash chromatography, it facilitates efficient access to indole-based scaffolds relevant to drug discovery programs.
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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-H317
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: