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Structure of 1896916-30-5
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This bench-stable, moisture-tolerant building block features a chlorinated triazolopyridine core paired with a reactive alcohol functionality. The electron-deficient heterocycle enables efficient coupling reactions, while the hydroxymethyl group facilitates direct incorporation into complex molecular architectures under standard conditions.
(7-Chloro-[1,2,4]triazolo[1,5-a]pyridin-2-yl)methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to triazolopyridine-based scaffolds. The primary alcohol functionality facilitates straightforward derivatization via oxidation, esterification, or coupling reactions. Its bench-stable nature and compatibility with common reaction conditions support reliable integration into medicinal chemistry workflows and API intermediate development.
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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: