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Structure of 1019021-93-2
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7-Bromoimidazo[1,2-a]pyridine-3-carboxylic acid features a fused heterocyclic core with a bromine substituent at the 7-position and a carboxylic acid group at the 3-position. This combination imparts enhanced reactivity for cross-coupling and derivatization, enabling direct incorporation into bioactive scaffolds. The molecule exhibits excellent stability under standard bench conditions and facilitates efficient functionalization in medicinal chemistry campaigns.
7-Bromoimidazo[1,2-a]pyridine-3-carboxylic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates amide bond formation and derivatization. The molecule exhibits good bench stability and compatibility with standard synthetic protocols, making it suitable for medicinal chemistry campaigns and process development in API synthesis.
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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: