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Structure of 1807072-92-9
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2-Bromo-3-fluoro-4-nitropyridine features a tri-functionalized pyridine core with distinct halogen and nitro groups enabling precise diversification in heterocyclic synthesis. The ortho-bromo and fluoro substituents facilitate palladium-catalyzed cross-coupling, while the electron-deficient nitro group enhances reactivity in nucleophilic substitution. This compound serves as a key intermediate in pharmaceutical and agrochemical development.
2-Bromo-3-fluoro-4-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The nitro group provides a handle for selective reduction and further functionalization, while the fluorine substituent enhances metabolic stability in downstream pharmaceutical scaffolds. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex pyridine derivatives used in medicinal chemistry and agrochemical development.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
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Lot numbers can be found on the outside label of a product: