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Structure of 1190318-72-9
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Methyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-5-carboxylate features a brominated pyrrolopyridine core with a methyl ester at the C5 position, enabling direct functionalization in cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the bench-stable ester group supports straightforward derivatization under standard conditions.
Methyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-5-carboxylate serves as a versatile building block for the synthesis of functionalized heterocycles and bioactive scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization via hydrolysis or nucleophilic substitution. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient integration into medicinal chemistry and process development 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-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: