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Structure of 603305-89-1
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7-Bromothieno[3,2-b]pyridine features a fused thienopyridine core with a bromine substituent at the 7-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical and materials architectures, offering enhanced stability and predictable reactivity under standard conditions.
7-Bromothieno[3,2-b]pyridine serves as a versatile building block in the synthesis of biologically active heterocycles and functional materials. Its bromine substituent enables facile palladium-catalyzed cross-coupling reactions, facilitating the construction of complex molecular architectures. The fused thienopyridine core offers enhanced planarity and electron-rich character, contributing to favorable π-stacking and redox properties. This compound exhibits excellent bench stability and compatibility with standard synthetic protocols, making it a reliable reagent for medicinal chemistry and materials science applications.
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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: