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Structure of 34552-13-1
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3-Amino-2-chloro-5-methylpyridine features a pyridine core bearing amino, chloro, and methyl substituents at strategic positions, enabling selective functionalization in heterocyclic synthesis. This electron-rich scaffold supports efficient coupling reactions under mild conditions, offering robust performance in pharmaceutical intermediates and agrochemical development.
3-Amino-2-chloro-5-methylpyridine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds through palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The amino and chloro groups provide orthogonal reactivity for sequential functionalization, while the methyl substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by recrystallization, it facilitates scalable synthesis of bioactive heterocycles and API intermediates.
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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-H318-H335
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Precautionary Statements : P261-P264-P270-P271-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: