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*For research and further manufacturing use only, not for direct human use.
Structure of 167884-17-5
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Imidazo[1,2-a]pyridin-5-ylmethanol delivers a rigid heteroaromatic scaffold with a reactive hydroxymethyl group, enabling direct functionalization in medicinal chemistry. This bench-stable, moisture-tolerant building block integrates efficiently into kinase inhibitors and bioactive scaffolds, offering enhanced solubility and metabolic stability in drug discovery applications.
Imidazo[1,2-a]pyridin-5-ylmethanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds through standard functional group transformations. Its bench-stable nature and compatibility with diverse reaction conditions facilitate straightforward derivatization, including oxidation to the aldehyde or esterification, supporting applications in medicinal chemistry and process 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-H320-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: