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Structure of 192189-16-5
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tert-Butyl 3-bromo-1H-pyrrolo[3,2-c]pyridine-1-carboxylate features a brominated pyrrolopyridine core with a bench-stable tert-butyl ester handle. This electrophilic scaffold enables direct coupling in cross-coupling reactions and integrates readily into complex heterocyclic architectures under standard conditions.
tert-Butyl 3-bromo-1H-pyrrolo[3,2-c]pyridine-1-carboxylate serves as a versatile building block for the synthesis of substituted pyrrolopyridine scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the tert-butyl ester provides stability and convenient deprotection under acidic conditions. Its compatibility with diverse functional groups and robust bench stability facilitate efficient access to complex heterocyclic architectures relevant in medicinal chemistry and materials science.
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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: