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Structure of 106854-77-7
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1-Bromo-4-(2,2,2-trifluoroethoxy)benzene features a bromine substituent and a trifluoroethoxy group positioned para to one another on the benzene ring. This electronic configuration enhances its utility in palladium-catalyzed cross-coupling reactions, where the electron-deficient aryl halide integrates efficiently with diverse nucleophiles. The trifluoroethoxy moiety imparts improved metabolic stability and lipophilicity, beneficial for medicinal chemistry applications.
1-Bromo-4-(2,2,2-trifluoroethoxy)benzene serves as a versatile aryl halide building block in cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The trifluoroethoxy group enhances metabolic stability and modulates electronic properties, while the bromine center provides high reactivity in Pd-catalyzed couplings. Bench-stable and compatible with standard purification protocols, it facilitates streamlined synthesis of fluorinated aromatic scaffolds relevant to agrochemical and pharmaceutical development.
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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: