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Structure of 915107-31-2
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Methyl 6-chloro-5-methoxynicotinate is a bench-stable, electron-deficient heterocyclic ester featuring a chloro group at the 6-position and a methoxy substituent at the 5-position. This structural motif enables efficient coupling in cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive nitrogen-containing compounds.
Methyl 6-chloro-5-methoxynicotinate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds. The ortho-chloro and methoxy groups facilitate directed metalation and selective functionalization, while the ester moiety supports further transformations including hydrolysis, reduction, or coupling reactions. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step syntheses of bioactive heterocycles 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: