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Structure of 110729-51-6
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2-Fluoro-N-methyl-5-nitroaniline features a fluorinated aromatic ring paired with an electron-deficient nitro group and a methylamino substituent, enabling efficient integration into diverse synthetic pathways. This bench-stable compound serves as a key building block for pharmaceutical intermediates and functional materials, offering enhanced reactivity in coupling and cyclization reactions under standard conditions.
2-Fluoro-N-methyl-5-nitroaniline serves as a versatile building block in medicinal chemistry, enabling the construction of fluorinated heterocycles and bioactive scaffolds. Its orthogonal functional groups—fluorine, nitro, and N-methyl amine—facilitate sequential transformations under standard conditions. The compound exhibits good bench stability and compatibility with common coupling reactions, supporting efficient synthesis of advanced intermediates for drug discovery programs.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: