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Structure of 1204298-60-1
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3-Bromo-5-methoxy-1H-pyrrolo[2,3-c]pyridine features a fused heterocyclic core with bromine and methoxy substituents positioned for selective functionalization. This electron-deficient scaffold enables efficient cross-coupling reactions and serves as a key building block in medicinal chemistry. The molecule exhibits robust stability under standard conditions and facilitates rapid diversification in drug discovery workflows.
3-Bromo-5-methoxy-1H-pyrrolo[2,3-c]pyridine serves as a versatile heterocyclic building block for C–H functionalization and cross-coupling reactions. The bromo group enables palladium-catalyzed coupling with boronic acids, amines, and other nucleophiles, while the methoxy substituent provides moderate electron donation and enhances solubility. This scaffold exhibits bench stability and compatibility with standard synthetic workflows, facilitating efficient access to substituted pyrrolopyridines used 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: