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Structure of 129912-22-7
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2-Methylimidazo[1,2-a]pyridine-6-carboxylic acid features a fused heterocyclic core with a carboxylic acid group at the 6-position, enabling direct conjugation or derivatization. The methyl substituent enhances electronic effects and steric profile, improving solubility and metabolic stability in synthetic applications. This scaffold serves as a key building block for bioactive molecules and ligands in medicinal chemistry.
2-Methylimidazo[1,2-a]pyridine-6-carboxylic acid serves as a versatile heterocyclic building block for medicinal chemistry and catalytic system development. Its fused imidazo-pyridine core provides robust structural rigidity and tunable basicity, enabling efficient derivatization via amide coupling, esterification, or metal-catalyzed cross-coupling reactions. The carboxylic acid functionality facilitates conjugation with biomolecules and supports purification via ion-exchange chromatography. Bench-stable and compatible with standard synthetic protocols, it functions as a key scaffold in the construction of bioactive molecules and functionalized ligands.
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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: