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Structure of 1261628-71-0
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4-Chloro-6-methoxypyridin-2-amine features a pyridine core functionalized with chlorine and methoxy groups, enabling selective coupling in medicinal chemistry. The ortho-chloro substituent facilitates palladium-catalyzed cross-coupling reactions, while the amino group serves as a direct handle for derivatization. This scaffold demonstrates stability under standard reaction conditions and compatibility with diverse synthetic transformations.
4-Chloro-6-methoxypyridin-2-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. The chloro group facilitates palladium-catalyzed cross-coupling reactions, while the methoxy and amino functionalities offer orthogonal handles for further derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for modular synthesis workflows in API development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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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: