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Structure of 63878-73-9
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(2-Fluoro-5-nitrophenyl)methanol features a fluorinated aromatic ring paired with a nitro group at the para position, delivering enhanced electrophilicity and stability. This configuration enables efficient coupling reactions in synthetic pathways, particularly in the construction of bioactive heterocycles and pharmaceutical intermediates under standard conditions.
(2-Fluoro-5-nitrophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling direct introduction of both fluorine and nitro functionality adjacent to a benzylic alcohol. Its bench-stable nature and compatibility with standard transformations—such as nucleophilic substitution, reduction of the nitro group, and derivatization of the alcohol—facilitate efficient access to diverse heterocyclic scaffolds and functionalized aryl 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: