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Structure of 190011-87-1
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3-Chloro-2,6-difluorobenzaldehyde features a trifluorinated aromatic core with orthogonal electron-withdrawing substituents that enhance electrophilicity at the carbonyl carbon. This configuration enables efficient coupling in cross-coupling reactions and facilitates rapid functionalization in pharmaceutical intermediates. The molecule exhibits excellent stability under standard handling conditions and demonstrates favorable solubility in common organic solvents.
3-Chloro-2,6-difluorobenzaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated aromatic scaffolds. Its orthogonal reactivity profile—driven by the electron-withdrawing chloro and difluoro substituents—facilitates nucleophilic addition, cross-coupling, and condensation reactions under standard conditions. The compound exhibits excellent bench stability and is readily purified via flash chromatography, making it well-suited for scalable synthesis of bioactive molecules and pharmaceutical intermediates.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352
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Lot numbers can be found on the outside label of a product: