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Structure of 58551-83-0
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2,4,6-Trifluorobenzaldehyde features a highly electron-deficient aromatic ring due to three fluorine substituents in the 2,4,6-positions. This strong inductive withdrawal enhances electrophilicity at the carbonyl carbon, enabling efficient nucleophilic addition reactions. The compound exhibits excellent bench stability and compatibility with moisture-sensitive transformations. It serves as a key building block for pharmaceutical intermediates and functional materials requiring fluorinated aromatic motifs.
2,4,6-Trifluorobenzaldehyde serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering enhanced electrophilicity at the carbonyl due to strong electron-withdrawing effects of the trifluoromethyl groups. Its bench-stable nature and compatibility with nucleophilic addition reactions facilitate efficient access to diverse heterocyclic scaffolds and functionalized aryl derivatives under standard reaction conditions.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362+P364
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Lot numbers can be found on the outside label of a product: