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Structure of 1159833-34-7
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3,6-Dimethylimidazo[1,2-a]pyridine-2-carboxylic acid features a rigid fused heterocyclic core with dual methyl substituents enhancing steric protection and electronic modulation. The carboxylic acid group enables direct conjugation or derivatization in synthetic sequences. This scaffold delivers high stability under standard conditions and integrates readily into advanced ligand designs for transition metal catalysis and pharmaceutical intermediates.
3,6-Dimethylimidazo[1,2-a]pyridine-2-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and catalysis research. Its fused imidazopyridine core provides enhanced rigidity and metabolic stability, while the carboxylic acid group enables direct derivatization or metal coordination. The methyl substituents at C3 and C6 improve solubility and facilitate downstream functionalization. This compound exhibits excellent bench stability and is compatible with standard coupling reactions, making it ideal for constructing complex scaffolds in drug discovery programs.
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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: