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Structure of 138642-96-3
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6-Chloro-2-methylimidazo[1,2-a]pyridine-3-carboxylic acid features a fused tricyclic core with complementary electron-withdrawing and steric elements. The carboxylic acid group enables direct derivatization, while the chloro and methyl substituents enhance reactivity in cross-coupling and bioconjugation workflows. This scaffold delivers robust stability under standard bench conditions.
6-Chloro-2-methylimidazo[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 methyl groups provide sites for further functionalization via cross-coupling or nucleophilic substitution. The molecule exhibits good bench stability and facilitates efficient purification, making it well-suited for medicinal chemistry campaigns and API intermediate 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: