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Structure of 56826-61-0
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This bench-stable (2-Methylpyridine-3-yl)methanol features a pyridyl scaffold with a pendant hydroxymethyl group, enabling direct functionalization or coupling reactions. The electron-rich heterocycle facilitates transition metal coordination, while the primary alcohol offers versatility in derivatization.
(2-Methylpyridine-3-yl)methanol serves as a versatile building block in medicinal chemistry and catalysis, enabling efficient functionalization at the pyridine ring via directed ortho-metalation. Its bench-stable aldehyde precursor functionality facilitates reductive amination, oxidation, and coupling reactions with high regioselectivity. The molecule functions effectively in transition-metal-catalyzed transformations and provides access to heterocyclic scaffolds relevant to pharmaceutical 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: