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Structure of 1638760-65-2
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Methyl 3-bromo-1H-pyrrolo[2,3-b]pyridine-6-carboxylate features a brominated pyrrolopyridine core with a methyl ester at the C6 position, offering a reactive handle for cross-coupling transformations. The electron-deficient heterocycle facilitates palladium-catalyzed functionalization, while the bench-stable ester group enables straightforward derivatization in synthetic sequences.
Methyl 3-bromo-1H-pyrrolo[2,3-b]pyridine-6-carboxylate serves as a versatile building block for constructing nitrogen-rich heterocyclic scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to complex pyrrolopyridine-based architectures 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: