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Structure of 660432-43-9
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This bench-stable reagent features a fluorinated aryl ring paired with a nitro group at the para position and a primary alcohol functionality. The electron-deficient aromatic system enhances reactivity in nucleophilic substitution, while the hydroxymethyl group enables straightforward derivatization. This combination supports efficient coupling in synthetic pathways requiring controlled activation.
(2-Fluoro-4-nitrophenyl)methanol serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of heterocyclic scaffolds and functionalized aryl derivatives. Its reactivity is enhanced by the synergistic electronic effects of the ortho-fluoro and para-nitro groups, facilitating nucleophilic aromatic substitution and directed metalation. The primary alcohol functionality provides a handle for derivatization, while the compound exhibits good bench stability and ease of purification—key attributes for industrial-scale synthesis and medicinal chemistry applications.
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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: