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Structure of 36131-43-8
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Ethyl 3-formyl-1H-pyrrole-2-carboxylate features a pyrrole core bearing both formyl and ester functionalities, enabling direct integration into heterocyclic synthesis. The electron-deficient pyrrole ring facilitates nucleophilic addition, while the formyl group serves as a key handle for C–C bond formation via aldol or Wittig reactions. This bench-stable reagent streamlines access to complex nitrogen-containing architectures in medicinal chemistry and materials science.
Ethyl 3-formyl-1H-pyrrole-2-carboxylate serves as a versatile heterocyclic building block for constructing biologically relevant scaffolds. The conjugated formyl and ester groups enable sequential functionalization, facilitating nucleophilic additions, condensation reactions, and transition-metal-catalyzed couplings. Its bench-stable nature and compatibility with common protecting group strategies make it ideal for iterative synthesis in medicinal chemistry and process development workflows.
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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: