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Structure of 688357-19-9
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Methyl 4-chloro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate features a fused heterocyclic core with a chlorinated pyridine ring and an ester-functionalized pyrrole moiety. This electron-deficient scaffold integrates readily into transition metal-catalyzed coupling reactions and serves as a key building block in the synthesis of bioactive alkaloids and pharmaceutical intermediates.
Methyl 4-chloro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrrolopyridine scaffolds prevalent in pharmaceutical research. The chloro group at the C4 position facilitates palladium-catalyzed cross-coupling reactions, while the ester functionality supports sequential transformations including hydrolysis and derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for iterative synthetic strategies in medicinal chemistry and process 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: