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Structure of 578-28-9
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1-Chloro-2,5-difluoro-4-nitrobenzene features a highly electron-deficient aromatic core stabilized by orthogonal fluorine and nitro substituents. This trifunctional scaffold enables direct coupling in cross-coupling reactions and facilitates site-specific derivatization under mild conditions. The chlorine moiety serves as a reactive handle for palladium-catalyzed transformations, while the para-nitro group enhances electrophilicity for nucleophilic substitution pathways.
1-Chloro-2,5-difluoro-4-nitrobenzene serves as a versatile electrophilic building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its activated aryl chloride functionality. The presence of ortho-fluorine substituents enhances reactivity in nucleophilic aromatic substitution processes, while the nitro group provides strong electron-withdrawal and facilitates downstream transformations. Its bench-stable nature and compatibility with diverse functional groups make it a practical choice for constructing complex heterocyclic scaffolds 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 : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: