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Structure of 317335-15-2
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Methyl 4-(hydroxymethyl)picolinate features a pyridine ring bearing a methyl ester and hydroxymethyl group at the 4-position, enabling direct functionalization. This bench-stable derivative integrates readily into synthetic sequences requiring polar, electron-deficient heterocycles with orthogonal reactivity.
Methyl 4-(hydroxymethyl)picolinate serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based scaffolds. The hydroxymethyl group facilitates direct functionalization or oxidation to carboxylic acid, while the methyl ester supports selective transformations under standard conditions. Its bench-stable nature and compatibility with common coupling and protection strategies make it ideal for modular synthesis workflows.
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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 : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: