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Structure of 64465-53-8
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4-Fluoro-3-methoxyaniline features a fluorinated aromatic ring bearing both methoxy and primary amine functionalities, enabling selective coupling in pharmaceutical synthesis. The electron-withdrawing fluorine at the para-position enhances reactivity in nucleophilic substitution processes. This bench-stable intermediate integrates readily into complex molecular architectures requiring directed functionalization.
4-Fluoro-3-methoxyaniline serves as a valuable building block in medicinal chemistry, enabling access to fluorinated aromatic scaffolds via standard coupling reactions. Its ortho-fluoro and meta-methoxy substituents provide directional control in electrophilic substitution and facilitate downstream functionalization. The compound exhibits good bench stability and compatibility with common protecting group strategies, simplifying purification and integration into multi-step syntheses.
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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#: 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-H318-H335-H412
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Precautionary Statements : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P310-P312-P330-P332+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: