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Structure of 843608-45-7
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This trifluoromethylated arylamine integrates a brominated phenyl moiety with a reactive amine handle, enabling direct coupling in cross-coupling and C–N bond formation. The electron-deficient aromatic ring enhances electrophilicity, while the bench-stable trifluoromethyl group improves metabolic resistance and lipophilic character for synthetic applications.
1-(3-Bromophenyl)-2,2,2-trifluoroethan-1-amine serves as a versatile building block for the synthesis of fluorinated aromatic amines. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the bromo substituent enables subsequent cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig couplings. The amine functionality provides a handle for derivatization, and the compound exhibits good bench stability and ease of purification, making it suitable for medicinal chemistry campaigns and process 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: