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Structure of 1264193-12-5
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6-Bromothiazolo[4,5-b]pyridine features a fused thiazolopyridine core with a bromine substituent at the 6-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and advanced materials, offering high stability under standard conditions and compatibility with palladium-catalyzed transformations.
6-Bromothiazolo[4,5-b]pyridine serves as a versatile building block for the synthesis of functionalized heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. Its bromine substituent facilitates efficient C–C and C–heteroatom bond formation, making it well-suited for constructing complex scaffolds in medicinal chemistry and materials science. The compound exhibits excellent bench stability and ease of purification, supporting reliable integration into multi-step synthetic sequences.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: