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Structure of 937-19-9
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Methyl 5-cyano-1H-pyrrole-2-carboxylate features a conjugated pyrrole core with strategically positioned electron-withdrawing cyano and ester groups. This combination enhances electrophilicity at the C2 position, enabling efficient coupling in transition-metal-catalyzed reactions. The molecule exhibits bench-stable handling characteristics and integrates readily into heterocyclic synthesis workflows.
Methyl 5-cyano-1H-pyrrole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrrole-based scaffolds through standard functional group manipulations. The cyano and ester groups provide orthogonal reactivity for nucleophilic addition, reduction, and coupling reactions, facilitating downstream derivatization. Its bench-stable nature and compatibility with common reaction conditions make it well-suited for medicinal chemistry campaigns and process-scale applications.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: