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Structure of 648423-85-2
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Imidazo[1,2-a]pyridine-7-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 7-position, enabling direct conjugation or derivatization. This scaffold combines enhanced planarity and electron-deficient character, ideal for pharmaceutical intermediates requiring metabolic stability and defined polarity. The acidic functionality supports salt formation and solubility tuning in synthetic workflows.
Imidazo[1,2-a]pyridine-7-carboxylic acid serves as a versatile scaffold in medicinal chemistry, enabling efficient access to bioactive heterocycles. Its carboxylic acid functionality facilitates direct amidation, esterification, and coupling reactions, supporting rapid library synthesis. The core structure exhibits favorable bench stability and functional group tolerance, making it well-suited for modular derivatization in drug discovery 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-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: