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Structure of 185331-69-5
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1-Bromo-2-fluoro-4-nitrobenzene features a trifunctional aryl scaffold with complementary electrophilic and electron-withdrawing groups. The bromine site enables palladium-catalyzed cross-coupling, while the ortho-fluorine facilitates nucleophilic aromatic substitution. This combination delivers efficient access to complex heterocycles and functionalized biaryls under mild conditions.
1-Bromo-2-fluoro-4-nitrobenzene serves as a versatile building block in nucleophilic aromatic substitution (SNAr) reactions, enabling efficient access to functionalized aryl intermediates. The ortho-fluorine and para-bromine substituents provide orthogonal reactivity, facilitating sequential substitutions under mild conditions. Its bench-stable nature and compatibility with diverse nucleophiles—such as amines, thiols, and alkoxides—make it ideal for constructing complex heterocycles and pharmaceutical scaffolds in medicinal chemistry workflows.
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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: