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Structure of 136592-20-6
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2-Bromo-1-(6-bromopyridin-3-yl)ethan-1-one features a dual brominated pyridine scaffold paired with an acetyl moiety, enabling direct incorporation into cross-coupling cascades. The electron-deficient aryl halide and reactive ketone group facilitate efficient palladium-catalyzed transformations under mild conditions. This bench-stable reagent serves as a key building block for functionalized heterocycles in medicinal chemistry and materials synthesis.
2-Bromo-1-(6-bromopyridin-3-yl)ethan-1-one serves as a versatile building block in cross-coupling chemistry, enabling efficient construction of biaryl and heterocyclic architectures. The dual bromine functionalities provide orthogonal reactivity for sequential palladium-catalyzed transformations, while the ketone moiety offers a handle for further functionalization. Bench-stable and compatible with standard reaction conditions, it facilitates reliable access to complex scaffolds in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P302+P352-P304+P340-P330-P362+P364-P363-P405-P501
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Lot numbers can be found on the outside label of a product: