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Structure of 454-78-4
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2-Bromo-1-chloro-4-(trifluoromethyl)benzene features a trifluoromethyl group that imparts strong electron-withdrawal and enhanced metabolic stability, while the bromo and chloro substituents enable selective cross-coupling reactions under standard conditions. This aryl halide serves as a key building block in pharmaceutical synthesis and materials chemistry.
2-Bromo-1-chloro-4-(trifluoromethyl)benzene serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the strategic placement of bromo and chloro substituents allows for sequential functionalization. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for scalable synthesis of complex aromatic scaffolds.
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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: