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Structure of 201849-13-0
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1-Bromo-3-chloro-2,4-difluorobenzene features a uniquely substituted aromatic ring enabling precise coupling reactions in pharmaceutical synthesis. The strategic placement of bromo, chloro, and difluoro groups facilitates selective cross-coupling under mild conditions. This electron-deficient aryl halide offers enhanced stability and predictable reactivity, streamlining access to complex fluorinated scaffolds in medicinal chemistry workflows.
1-Bromo-3-chloro-2,4-difluorobenzene serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its complementary halogen reactivity. The strategic placement of bromo, chloro, and difluoro substituents provides orthogonal functionalization potential, facilitates selective transformations, and enhances metabolic stability in target scaffolds. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for multi-step synthetic sequences.
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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: