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Structure of 85118-24-7
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2-Bromo-4-(trifluoromethyl)benzaldehyde features a bromine atom at the ortho position and a trifluoromethyl group at the para position relative to the aldehyde functional group. This electron-deficient aromatic scaffold enables efficient coupling in cross-coupling reactions, particularly in Suzuki-Miyaura and Negishi transformations. The molecule exhibits enhanced stability under standard bench conditions and demonstrates compatibility with diverse reaction environments.
2-Bromo-4-(trifluoromethyl)benzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromo and aldehyde functionalities. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the aldehyde facilitates imine formation and reductive amination. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for synthesizing functionalized heterocycles and advanced intermediates.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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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 : H319-H411
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Precautionary Statements : P264-P273-P280-P305+P351+P338-P337+P313-P391-P501
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Lot numbers can be found on the outside label of a product: