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Structure of 720666-45-5
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2-Chloro-5-methoxypyridin-3-amine features a pyridine core functionalized with chlorine, methoxy, and amine groups, enabling selective coupling in medicinal chemistry. The electron-deficient ring facilitates nucleophilic substitution, while the amine handles serve as anchor points for diversification. This scaffold offers stability under standard conditions and compatibility with common transition-metal-catalyzed reactions.
2-Chloro-5-methoxypyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive chloropyridine moiety. The methoxy and amino groups provide orthogonal functional handles for further derivatization, while the compound exhibits excellent bench stability and compatibility with standard purification methods. It functions as a key intermediate in the synthesis of heterocyclic scaffolds relevant to pharmaceutical 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: