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Structure of 252004-45-8
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4-Chloro-2,6-difluorobenzaldehyde features a trifluorinated aromatic core with orthogonal electron-withdrawing substituents, enabling precise tuning of reactivity in cross-coupling and electrophilic substitution processes. The aldehyde functionality provides a handle for rapid derivatization, while the fluorine atoms enhance metabolic stability and modulate electronic properties. This compound exhibits excellent bench stability and compatibility with diverse reaction conditions.
4-Chloro-2,6-difluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds via nucleophilic addition and condensation reactions. Its electron-deficient aromatic ring enhances reactivity in coupling processes, while the aldehyde functionality offers direct access to imines, hydrazones, and amides. Bench-stable and compatible with standard purification methods, it facilitates scalable synthesis workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: