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Structure of 261762-39-4
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2-Chloro-3,6-difluorobenzaldehyde features a trifluorinated aromatic core with a reactive aldehyde group, enabling efficient coupling in cross-coupling and Ullmann-type reactions. The electron-deficient ring enhances electrophilicity, while the ortho-chloro and meta-fluoro substituents provide steric and electronic control for selective functionalization. This bench-stable reagent integrates readily into complex molecular architectures under standard conditions.
2-Chloro-3,6-difluorobenzaldehyde serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of fluorinated heterocycles and substituted aromatic scaffolds. Its ortho-chloro and meta-difluoro substitution pattern provides enhanced metabolic stability and modulates electronic properties, while the aldehyde functionality facilitates nucleophilic addition, reductive amination, and Ullmann-type coupling reactions. Bench-stable and amenable to standard purification techniques, it functions reliably in multi-step syntheses requiring precise regiocontrol.
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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-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: