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Structure of 1205671-72-2
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Methyl 6-chloro-5-(hydroxymethyl)picolinate features a strategically positioned chloro group and a hydroxymethyl side chain on the picolinate scaffold, enabling selective functionalization in synthetic routes. This bench-stable derivative integrates readily into complex molecular architectures, offering enhanced solubility and compatibility in transition metal-catalyzed transformations.
Methyl 6-chloro-5-(hydroxymethyl)picolinate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized heterocyclic scaffolds. The hydroxymethyl group facilitates selective derivatization via oxidation, protection, or substitution reactions, while the chloro and ester functionalities support further transformations such as nucleophilic displacement or cross-coupling. Its bench-stable nature and compatibility with standard purification methods make it well-suited for medicinal chemistry and process development 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 : H302-H315-H319-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: