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Structure of 98121-41-6
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3-Amino-5,6-dichloropyridine features a pyridine core functionalized with amino and dichloro substituents at strategic positions, enabling selective coupling reactions. The electron-deficient ring system enhances reactivity in nucleophilic substitution processes, while the amino group provides a handle for further derivatization. This compound serves as a key intermediate in medicinal chemistry and agrochemical synthesis, offering high stability under standard bench conditions.
3-Amino-5,6-dichloropyridine serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted pyridine scaffolds via Suzuki-Miyaura and Buchwald-Hartwig coupling reactions. Its ortho-dichloro substitution pattern facilitates selective functionalization, while the amino group offers direct derivatization potential. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it well-suited for scalable synthesis of API intermediates and heterocyclic libraries.
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GHS Pictogram :
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GHS No : GHS05,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-H318
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: