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Structure of 51984-46-4
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(3-Methoxypyridin-2-yl)methanol features a pyridine ring bearing a methoxy group at the 3-position and a hydroxymethyl substituent at the 2-position. This configuration imparts enhanced solubility and stability under standard conditions, enabling direct incorporation into synthetic sequences without protective group manipulation. The compound serves as a key building block for bioactive heterocycles and functionalized ligands in medicinal chemistry applications.
(3-Methoxypyridin-2-yl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to functionalized pyridine derivatives. Its pendant hydroxymethyl group facilitates straightforward derivatization via oxidation, etherification, or coupling reactions. The molecule exhibits good bench stability and compatibility with common protecting group strategies, making it suitable for multi-step synthesis workflows requiring orthogonality and predictable reactivity.
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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: