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Structure of 36131-46-1
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Ethyl 5-nitro-1H-pyrrole-2-carboxylate features a bench-stable, electron-deficient pyrrole core with a strategically positioned nitro group enhancing reactivity in cross-coupling and cycloaddition processes. This ester functionality enables direct incorporation into complex heterocyclic architectures under standard conditions, offering a reliable entry point for synthetic medicinal chemistry and materials development.
Ethyl 5-nitro-1H-pyrrole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles via reduction, coupling, or cyclization reactions. The nitro group at C5 facilitates selective functionalization, while the ester moiety supports further transformations such as hydrolysis or amidation. Its bench-stable nature and compatibility with standard reaction conditions 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: