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Structure of 40611-79-8
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Methyl 4-formyl-1H-pyrrole-2-carboxylate features a pyrrole core with strategically positioned formyl and ester groups, enabling direct incorporation into heterocyclic scaffolds. The electron-deficient pyrrole ring supports efficient transition metal-catalyzed coupling reactions, while the formyl moiety offers a versatile handle for reductive amination or condensation chemistry. This bench-stable reagent streamlines access to complex nitrogen-containing architectures in synthetic and medicinal chemistry workflows.
Methyl 4-formyl-1H-pyrrole-2-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and materials synthesis. The ortho-aldehyde and ester functionalities enable sequential functionalization, including reductive amination, Suzuki-Miyaura coupling, and condensation reactions. Bench-stable and readily purified by column chromatography, it facilitates efficient access to substituted pyrroles and fused polycyclic scaffolds relevant to API development.
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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: