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Structure of 221198-99-8
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3-Fluoro-4-(4-methylpiperazin-1-yl)aniline features a fluorinated aromatic core paired with a sterically accessible piperazine handle, enabling efficient conjugation in medicinal chemistry. The electron-rich amine moiety facilitates rapid derivatization under standard coupling conditions. This scaffold supports target engagement in kinase inhibitor design and CNS-targeted drug discovery.
3-Fluoro-4-(4-methylpiperazin-1-yl)aniline serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive heterocycles and kinase inhibitor scaffolds. The aniline functionality facilitates direct coupling reactions, while the fluorine substituent enhances metabolic stability and modulates electronic properties. The 4-methylpiperazinyl group provides solubility and hydrogen-bonding capacity, supporting drug-like properties. This compound exhibits bench stability and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns 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: