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Structure of 21801-79-6
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This heterocyclic carboxylic acid features a fused imidazo[1,2-a]pyridine core with a methyl substituent at the 2-position, enhancing electronic delocalization and solubility. The carboxylic acid group enables direct coupling in peptide synthesis or metal coordination. Designed for medicinal chemistry applications, it offers improved metabolic stability and targeted receptor binding compared to non-substituted analogs.
2-Methylimidazo[1,2-a]pyridine-3-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and catalytic system development. Its fused tricyclic core provides enhanced rigidity and defined spatial orientation, enabling precise molecular positioning in target-directed synthesis. The carboxylic acid functionality facilitates direct amidation, esterification, or metal coordination, while the methyl group enhances metabolic stability and modulates lipophilicity. This compound exhibits good bench stability and compatibility with standard purification techniques, making it suitable for iterative synthetic workflows and API intermediate construction.
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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: