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Structure of 1001070-33-2
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This brominated pyrrolopyridine scaffold features a benzenesulfonyl group at the 1-position, enhancing solubility and electronic modulation. The para-bromo substituent enables facile cross-coupling reactions, facilitating rapid diversification in medicinal chemistry applications. Bench-stable and compatible with standard coupling conditions, this intermediate streamlines access to complex heterocyclic architectures.
1-(Benzenesulfonyl)-5-bromo-1H-pyrrolo[2,3-b]pyridine serves as a versatile building block for constructing nitrogen-containing heterocycles in medicinal chemistry. The benzenesulfonyl group enhances solubility and stability, while the bromo substituent enables palladium-catalyzed cross-coupling reactions. This compound exhibits excellent bench stability and facilitates efficient functionalization in standard synthetic 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-H319
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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: