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Structure of 40611-85-6
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Ethyl 4-methyl-1H-pyrrole-2-carboxylate features a bench-stable pyrrole core with an electron-rich heterocyclic ring, enabling direct functionalization at the C2 position. The ester group facilitates selective derivatization, while the methyl substituent enhances solubility and reactivity in cross-coupling and cycloaddition processes. This building block integrates efficiently into complex molecular architectures.
Ethyl 4-methyl-1H-pyrrole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles via standard functional group manipulations. Its ester group facilitates selective transformations, while the methyl substituent enhances regiochemical control. The compound exhibits good bench stability and compatibility with common coupling reactions, making it well-suited for 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: