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Structure of 914347-91-4
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Ethyl 3-fluoro-4-nitrobenzoate features a fluorinated aromatic ring paired with complementary nitro and ester functionalities, enabling selective coupling in cross-coupling reactions. The electron-deficient aryl moiety facilitates efficient palladium-catalyzed transformations, while the ethyl ester group supports downstream derivatization. This bench-stable reagent integrates readily into synthetic sequences requiring orthogonal functional handles.
Ethyl 3-fluoro-4-nitrobenzoate serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to functionalized aromatic scaffolds. The ortho-fluoro and para-nitro substituents provide complementary reactivity for nucleophilic substitution, metal-catalyzed coupling, and sequential reduction strategies. Its bench-stable nature and compatibility with standard purification methods make it well-suited for multi-step synthesis 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: