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Structure of 1306763-53-0
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Methyl 3-bromo-5-(trifluoromethoxy)benzoate features a bromine atom at the meta position relative to the ester, paired with a strongly electron-withdrawing trifluoromethoxy group at the para position. This combination enhances electrophilic reactivity while maintaining stability under standard conditions, enabling efficient coupling in cross-coupling reactions. The molecule’s bench-stable nature and solubility profile support straightforward integration into synthetic workflows for pharmaceutical intermediates and functional materials.
Methyl 3-bromo-5-(trifluoromethoxy)benzoate serves as a versatile building block in medicinal chemistry and materials synthesis, enabling palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. The trifluoromethoxy group imparts enhanced metabolic stability and lipophilicity, while the bromo substituent provides a reliable handle for further functionalization. Bench-stable and compatible with standard purification methods, it facilitates efficient access to complex aromatic scaffolds and fluorinated heterocycles used in API 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-H320-H335
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: