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Structure of 51984-71-5
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Ethyl 2-methyl-5-nitro-3-pyridinecarboxylate features a pyridine core bearing electron-deficient nitro and methyl substituents, enabling selective coupling reactions. The ester functionality facilitates downstream transformations in heterocyclic synthesis, while the bench-stable structure supports reliable handling under standard conditions.
Ethyl 2-methyl-5-nitro-3-pyridinecarboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine derivatives via standard functional group manipulations. Its nitro group facilitates reduction and subsequent coupling reactions, while the ester moiety supports hydrolysis, amidation, or cross-coupling transformations. The molecule exhibits good bench stability and compatibility with common reaction conditions, making it valuable for medicinal chemistry campaigns and process development workflows requiring robust pyridine scaffold elaboration.
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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: