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Structure of 1216294-32-4
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This bench-stable, moisture-tolerant building block features a fused imidazopyridine core with a reactive hydroxymethyl group. The electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and enables direct derivatization for bioactive compound synthesis under standard conditions.
(7-Methylimidazo[1,2-a]pyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to imidazopyridine-based scaffolds. Its benzylic alcohol functionality facilitates direct oxidation to carboxylic acids or conversion to esters and other derivatives, supporting downstream functionalization. The molecule exhibits good bench stability and compatibility with standard coupling reactions, making it well-suited for modular synthesis of targeted bioactive compounds.
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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: