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Structure of 1261884-16-5
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4-Chloro-6-methoxypyridin-3-amine features a pyridine core functionalized with a chloro group at C4 and a methoxy substituent at C6, creating a uniquely electron-deficient heterocyclic scaffold. This arrangement enables selective coupling reactions in medicinal chemistry, particularly in the synthesis of kinase inhibitors and antiviral agents. The compound exhibits bench-stable handling under standard conditions and integrates efficiently into diverse reaction cascades.
4-Chloro-6-methoxypyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the methoxy and amine functionalities provide orthogonal handles for further functionalization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for modular synthesis of bioactive molecules.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: