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Structure of 503315-74-0
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(3-Fluoro-4-nitrophenyl)methanol features a fluorinated aromatic ring paired with a nitro group at the para position, enhancing electrophilicity and enabling selective functionalization. The benzylic alcohol moiety offers a handle for derivatization, while the molecule exhibits stability under standard bench conditions. This combination supports efficient integration into complex synthetic sequences.
(3-Fluoro-4-nitrophenyl)methanol serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated aromatic scaffolds. Its dual nitro and hydroxymethyl functionalities facilitate sequential transformations—nitro reduction followed by coupling or functionalization—while the fluorine substituent enhances metabolic stability and modulates electronic properties. Bench-stable and readily purified by column chromatography, it functions reliably in standard cross-coupling and reductive amination protocols.
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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: