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Structure of 681435-09-6
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2,4-Dichloro-6-fluorobenzaldehyde features a highly electron-deficient aromatic ring stabilized by orthogonal halogen substituents. This combination enhances reactivity in nucleophilic addition and coupling processes. The aldehyde group enables direct functionalization or integration into complex molecular architectures under mild conditions. Bench-stable and moisture-tolerant, it serves as a key building block for pharmaceutical intermediates and agrochemicals.
2,4-Dichloro-6-fluorobenzaldehyde 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 core enhances reactivity in Suzuki-Miyaura coupling and imine formation, while the orthogonal halogen substituents allow for selective functionalization. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable process development.
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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-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: