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Structure of 1211538-09-8
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Ethyl 6-methyl-5-nitropyridine-3-carboxylate features a pyridine core bearing a nitro group at C5 and a methyl substituent at C6, enabling strategic functionalization in heterocyclic synthesis. The ester handle facilitates coupling reactions, while the electron-deficient ring supports nucleophilic substitution under mild conditions. This compound serves as a key intermediate in medicinal chemistry and agrochemical development.
Ethyl 6-methyl-5-nitropyridine-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via sequential reduction and functionalization. The nitro group facilitates controlled reduction to an amine, while the ester supports amidation, hydrolysis, or coupling reactions. Its bench-stable nature and compatibility with standard synthetic protocols make it ideal 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-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: