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Structure of 949922-62-7
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tert-Butyl 2-bromo-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate features a brominated dihydrothienopyridine core with a tert-butyl ester handle, enabling direct incorporation into cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed functionalization, while the bench-stable ester group supports straightforward deprotection and derivatization under standard conditions.
tert-Butyl 2-bromo-6,7-dihydrothieno[3,2-c]pyridine-5(4H)-carboxylate serves as a versatile building block for the synthesis of thienopyridine-based scaffolds, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromo group facilitates C–C bond formation under standard conditions, while the tert-butyl ester offers stability and ease of subsequent deprotection. Its defined stereochemistry and bench-stable nature support reliable use in 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: