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Structure of 22940-71-2
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This bench-stable (5-methylpyridin-2-yl)methanol features a pyridine ring bearing a methyl group at the 5-position and a primary alcohol at the 2-position, enabling direct functionalization. The electron-rich aromatic system enhances reactivity in coupling processes, while the hydroxymethyl handle facilitates derivatization under standard conditions.
(5-Methylpyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient functionalization via oxidation to the corresponding aldehyde or carboxylic acid. Its pyridine ring provides strong coordination capacity for metal catalysts, while the benzylic alcohol functionality supports selective derivatization under mild conditions. The molecule exhibits excellent bench stability and compatibility with common protecting group strategies, facilitating its use in multi-step synthesis of heterocyclic scaffolds and drug candidates.
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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: