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Structure of 486460-26-8
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(4-Bromo-2,5-difluorophenyl)methanol features a trifunctional aromatic core bearing bromo and two fluorine substituents that enable selective cross-coupling and electrophilic functionalization. The pendant hydroxymethyl group offers direct access to aldehyde or carboxylic acid derivatives under mild oxidation conditions. This bench-stable reagent integrates readily into complex molecular architectures requiring halogen-directed C–H activation or metal-mediated coupling strategies.
(4-Bromo-2,5-difluorophenyl)methanol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient late-stage functionalization via cross-coupling and nucleophilic substitution reactions. Its benzylic alcohol functionality offers controlled reactivity, while the ortho-fluoro and para-bromo substituents provide orthogonal handles for sequential transformations. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable synthetic 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: