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Structure of 872181-59-4
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1-(3,5-Difluorophenyl)ethan-1-ol features a sterically accessible hydroxyl group flanked by two electron-withdrawing fluorine atoms, enhancing its stability and reactivity in synthetic transformations. This bench-stable phenolic alcohol integrates readily into complex molecular architectures, serving as a key intermediate in pharmaceutical and agrochemical development.
1-(3,5-Difluorophenyl)ethan-1-ol serves as a valuable building block in medicinal chemistry, offering a stable, bench-ready arylalkanol scaffold with enhanced metabolic stability due to fluorine substitution. The primary alcohol functionality enables straightforward derivatization via esterification, etherification, or oxidation to the corresponding aldehyde or carboxylic acid. Its compatibility with standard coupling reactions and tolerance of diverse functional groups make it a practical intermediate for synthesizing fluorinated heterocycles and bioactive molecules.
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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 : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: