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Structure of 1216142-18-5
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6-Chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid features a rigid fused heterocyclic core with complementary electron-withdrawing and alkyl substituents. This configuration enhances solubility in polar solvents while maintaining thermal stability under standard reaction conditions. The carboxylic acid group enables direct coupling reactions without additional activation, streamlining synthetic access to bioactive analogs in medicinal chemistry campaigns.
6-Chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid serves as a versatile building block for constructing bioactive heterocyclic scaffolds. Its carboxylic acid functionality enables direct coupling reactions, while the chloro and ethyl substituents provide orthogonal handles for further functionalization. The molecule exhibits bench stability and facilitates efficient derivatization in standard synthetic workflows, making it well-suited for medicinal chemistry campaigns targeting kinase inhibitors and other pharmaceutical leads.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: