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Structure of 226410-00-0
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Methyl 3-chloro-1H-pyrrole-2-carboxylate features a chlorinated pyrrole core with a methyl ester at the C2 position, enabling direct incorporation into heterocyclic synthesis. The electron-deficient pyrrole ring facilitates electrophilic substitution and serves as a key building block in medicinal chemistry scaffolds. This bench-stable reagent offers predictable reactivity under standard conditions for coupling and functionalization workflows.
Methyl 3-chloro-1H-pyrrole-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyrroles via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The chloro group at the C3 position offers high reactivity for functionalization, while the ester moiety provides stability and ease of purification. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal 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-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: