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Structure of 85686-97-1
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1,2-difluoro-4,5-dinitrobenzene features a highly electron-deficient aromatic core, enabling efficient nucleophilic aromatic substitution reactions. The ortho-fluorine atoms facilitate sequential displacement under mild conditions, while the para-nitro groups enhance reactivity and stabilize intermediates. This compound serves as a robust building block for functionalized heterocycles and advanced materials synthesis.
1,2-Difluoro-4,5-dinitrobenzene serves as a versatile electrophilic building block in nucleophilic aromatic substitution (SNAr) reactions, enabling efficient introduction of diverse amine and thiol functionalities under mild conditions. Its high reactivity stems from the synergistic electron-withdrawing effects of the dinitro and difluoro substituents, facilitating clean functionalization with excellent regiocontrol. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for use in the synthesis of complex heterocycles, pharmaceutical intermediates, and advanced materials.
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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 : H302-H315-H319-H341
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Precautionary Statements : P264-P280-P501
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Lot numbers can be found on the outside label of a product: