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Structure of 60186-13-2
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2,4,6-Trichloro-3-nitropyridine features a highly electron-deficient pyridine core stabilized by three chlorine substituents and a nitro group at the 3-position. This configuration enables selective coupling reactions in synthetic organic chemistry, particularly in the construction of heterocyclic scaffolds under mild conditions. The compound exhibits excellent bench stability and compatibility with diverse reaction environments.
2,4,6-Trichloro-3-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling selective functionalization at the 3-position via nucleophilic substitution. Its electron-deficient pyridine core facilitates robust reactivity with amines, thiols, and other nucleophiles under mild conditions. The molecule exhibits excellent bench stability and ease of purification, making it well-suited for scalable synthesis of advanced intermediates 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-H315-H319-H335
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: