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Structure of 25194-01-8
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2,6-Dichloro-4-nitropyridine features a pyridine core functionalized with two chlorine atoms at the 2 and 6 positions and a nitro group at the 4 position. This electron-deficient heterocycle integrates readily into cross-coupling reactions, serving as a robust building block for pharmaceutical intermediates and agrochemicals under standard conditions.
2,6-Dichloro-4-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient functionalization at the 4-position via nucleophilic substitution. The electron-deficient pyridine ring facilitates regioselective reactions with amines, thiols, and other nucleophiles, while the dichloro substituents offer orthogonal reactivity for sequential transformations. Its bench stability and ease of purification make it well-suited for iterative synthesis of complex scaffolds relevant to medicinal chemistry and agrochemical development.
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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#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H317-H318-H335
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Precautionary Statements : P261-P264-P270-P271-P272-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: