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Structure of 915107-30-1
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Methyl 6-chloro-5-hydroxynicotinate features a strategically positioned hydroxyl group and chloro substituent on the pyridine ring, enabling selective functionalization in medicinal chemistry. This bench-stable derivative integrates readily into synthetic routes requiring electron-deficient heterocyclic scaffolds.
Methyl 6-chloro-5-hydroxynicotinate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds. The pendant hydroxyl group facilitates direct derivatization via esterification, etherification, or oxidation, while the chloro substituent supports palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with common protecting group strategies streamline synthesis workflows for heterocyclic compounds and API intermediates.
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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: