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Structure of 261723-32-4
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(3-Bromo-2-fluorophenyl)methanol features a strategically positioned bromine and fluorine substituent on the aromatic ring, enabling selective functionalization in cross-coupling reactions. The benzylic alcohol moiety offers a reactive handle for derivatization, while the molecule exhibits excellent stability under standard handling conditions.
(3-Bromo-2-fluorophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling direct introduction of a brominated aryl alcohol motif. Its stability under standard handling conditions and compatibility with palladium-catalyzed cross-coupling reactions facilitate efficient C–C bond formation. The ortho-fluoro and meta-bromo substituents provide orthogonal reactivity for downstream functionalization, supporting modular synthesis of complex heterocyclic scaffolds and pharmaceutical intermediates.
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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: