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Structure of 160538-51-2
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3-Fluoro-4-nitrobenzaldehyde features a fluorinated aromatic ring paired with electron-withdrawing nitro and aldehyde groups, enabling precise tuning of reactivity in cross-coupling and condensation reactions. This bench-stable compound integrates readily into complex molecular architectures under standard conditions.
3-Fluoro-4-nitrobenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization at the aldehyde and nitro positions. Its electron-deficient aromatic core facilitates nucleophilic addition and transition-metal-catalyzed coupling reactions. The fluorine substituent enhances metabolic stability and modulates electronic properties, while the aldehyde group permits facile derivatization via reductive amination or imine formation. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses of heterocyclic scaffolds and 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P301+P310-P302+P352-P304+P341-P312-P330-P363-P501
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Lot numbers can be found on the outside label of a product: