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Structure of 1227268-77-0
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This heterocyclic carboxylic acid features a fused imidazo[1,2-a]pyridine core with a methyl substituent at the 3-position, delivering enhanced solubility and stability under standard conditions. The carboxylate group enables direct conjugation in medicinal chemistry scaffolds, while the electron-deficient aromatic system supports efficient coupling reactions.
3-Methylimidazo[1,2-a]pyridine-2-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and catalytic system development. Its fused imidazo[1,2-a]pyridine core provides enhanced rigidity and π-conjugation, enabling robust interactions in target binding. The carboxylic acid group facilitates direct derivatization or salt formation, supporting purification and solubility modulation. Bench-stable and compatible with standard coupling reactions, it functions effectively in the synthesis of advanced scaffolds and functional materials.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: