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Structure of 94191-15-8
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2-Bromothieno[3,2-b]pyridine features a fused thienopyridine core with a bromine substituent at the 2-position, enabling direct functionalization in cross-coupling reactions. The electron-deficient heterocycle integrates readily into pharmaceutical and agrochemical scaffolds, offering high reactivity under standard palladium-catalyzed conditions. This bench-stable, moisture-tolerant compound serves as a key building block for advanced synthetic intermediates.
2-Bromothieno[3,2-b]pyridine serves as a versatile building block in the synthesis of biologically active heterocycles and functional materials. The bromine substituent enables facile palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Stille couplings, facilitating the construction of complex molecular architectures. Its fused thienopyridine core exhibits excellent bench stability and compatibility with diverse functional groups, making it well-suited for iterative synthetic strategies 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: