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Structure of 320-49-0
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2-Bromo-5-hydroxybenzotrifluoride features a trifluoromethyl group flanked by bromo and hydroxyl substituents, enabling direct functionalization in late-stage synthesis. This electron-deficient aryl scaffold supports palladium-catalyzed cross-coupling and facilitates incorporation into bioactive molecules requiring fluorinated aromatic motifs.
2-Bromo-5-hydroxybenzotrifluoride serves as a versatile building block for the synthesis of fluorinated aromatic scaffolds, enabling direct coupling reactions via its bromine and hydroxyl functionalities. The trifluoromethyl group enhances metabolic stability and lipophilicity, while the ortho-hydroxybromide arrangement facilitates sequential functionalization in medicinal chemistry and materials science applications. Its bench-stable nature supports reliable handling and purification in multi-step syntheses.
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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: