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Structure of 1211541-93-3
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5-Fluoro-2-methoxypyridin-3-amine features a pyridine core with strategically positioned fluorine and methoxy groups, enabling enhanced electron-withdrawing effects and improved metabolic stability. This bench-stable compound integrates readily into medicinal chemistry scaffolds, serving as a key building block for kinase inhibitors and bioactive heterocycles.
5-Fluoro-2-methoxypyridin-3-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based pharmacophores. The ortho-fluoro and amino groups facilitate directed metalation and palladium-catalyzed coupling reactions, while the methoxy substituent enhances solubility and modulates electronic properties. Bench-stable and compatible with standard synthetic protocols, it functions effectively in the construction of kinase inhibitors and CNS-targeted compounds.
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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: