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Structure of 145325-40-2
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Methyl 4-bromothieno[2,3-c]pyridine-2-carboxylate features a fused thienopyridine core with a brominated position at the 4-site and an ester handle at the 2-position. This scaffold integrates readily into cross-coupling workflows, offering high stability under standard conditions and enabling efficient access to complex heterocyclic architectures in medicinal chemistry and materials science.
Methyl 4-bromothieno[2,3-c]pyridine-2-carboxylate serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the ester group offers compatibility with reduction and functionalization protocols. This compound exhibits bench stability and facilitates efficient synthesis of thienopyridine-based intermediates used in medicinal chemistry and materials science.
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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: