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Structure of 607373-83-1
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2-Chloro-4-methoxy-5-nitropyridine features a nitro group at C5 and a chloro substituent at C2, creating a highly electron-deficient pyridine core. This configuration enables direct coupling in cross-coupling reactions, while the methoxy group enhances solubility and modulates reactivity. The compound serves as a key intermediate in the synthesis of bioactive heterocycles.
2-Chloro-4-methoxy-5-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The ortho-chloro group exhibits high reactivity in Suzuki, Stille, and Buchwald–Hartwig transformations, while the methoxy and nitro substituents provide orthogonal handles for selective derivatization. Bench-stable and compatible with standard purification protocols, it facilitates the construction of complex pyridine-based scaffolds relevant to medicinal chemistry and agrochemical development.
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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: