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Structure of 400877-57-8
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Methyl 1-methyl-4-nitro-1H-pyrazole-3-carboxylate features a nitro-substituted pyrazole core paired with a methyl ester, enabling direct integration into heterocyclic synthesis. The electron-deficient pyrazole ring facilitates nucleophilic substitution, while the bench-stable ester group supports straightforward derivatization under standard conditions.
Methyl 1-methyl-4-nitro-1H-pyrazole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to functionalized pyrazole scaffolds. The nitro group facilitates subsequent reduction and coupling reactions, while the ester moiety supports orthogonal transformations. Its bench-stable nature and compatibility with standard synthetic protocols 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-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: