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Structure of 177420-63-2
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This trifluoromethyl-substituted benzoic acid features a bromine atom at the ortho position, enabling direct functionalization in cross-coupling reactions. The electron-withdrawing trifluoromethyl group enhances reactivity and stability, making it ideal for synthesizing bioactive compounds and advanced materials under standard conditions.
2-Bromo-3-(trifluoromethyl)benzoic acid serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromo group and electron-withdrawing trifluoromethyl substituent. The carboxylic acid functionality facilitates direct derivatization or incorporation into heterocyclic scaffolds. Its bench-stable solid form supports straightforward handling and purification, making it well-suited for iterative synthesis 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: