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Structure of 405230-82-2
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2,5-Dichloropyridin-4-amine features a pyridine core bearing two chlorine substituents at the 2 and 5 positions and an amino group at the 4-position. This electron-deficient heterocycle serves as a key building block in medicinal chemistry, enabling direct coupling reactions through its nucleophilic amine and halogenation sites. The molecule exhibits enhanced stability under standard conditions and facilitates efficient diversification in target-oriented synthesis.
2,5-Dichloropyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 4-position via nucleophilic substitution. Its dichloro substitution pattern provides orthogonal reactivity for sequential coupling processes, while the amine group facilitates amidation, sulfonamide formation, and transition-metal-catalyzed cross-couplings. The compound exhibits excellent bench stability and is readily purified by recrystallization, making it ideal for scalable synthesis of heterocyclic scaffolds found in agrochemicals and pharmaceuticals.
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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 : Ⅱ
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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: