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Structure of 1211596-19-8
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6-Bromopyrazolo[1,5-a]pyridine-3-carboxylic acid features a brominated pyrazolopyridine core paired with a carboxylic acid group, enabling direct conjugation or derivatization in synthetic workflows. The electron-deficient heterocycle facilitates cross-coupling reactions, while the carboxylic acid serves as a handle for amide formation or metal chelation. This compound offers robust stability under standard conditions and integrates efficiently into complex molecular architectures for medicinal chemistry applications.
6-Bromopyrazolo[1,5-a]pyridine-3-carboxylic acid serves as a versatile building block for the synthesis of biologically active heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo and carboxylic acid functionalities. The molecule exhibits bench stability and facilitates efficient derivatization via amide formation or esterification, supporting applications in medicinal chemistry and API development.
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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: