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Structure of 1086064-49-4
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4-Bromo-1H-pyrrolo[2,3-b]pyridin-2(3H)-one features a fused heterocyclic core with a bromine substituent at the 4-position, enabling direct functionalization in cross-coupling reactions. The lactam moiety imparts stability and polarity, facilitating solubility in common organic solvents. This scaffold serves as a key intermediate in medicinal chemistry for constructing bioactive compounds, particularly within kinase inhibitor and antiviral research.
4-Bromo-1H-pyrrolo[2,3-b]pyridin-2(3H)-one serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the lactam functionality offers hydrogen bonding capacity and structural rigidity. This compound exhibits good bench stability and facilitates efficient functionalization in late-stage diversification strategies common in medicinal chemistry.
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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: