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Structure of 193290-80-1
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3-Fluoro-4-formylbenzoic acid features a formyl group adjacent to a carboxylic acid, enabling direct coupling reactions. The ortho-fluorine enhances electrophilicity and facilitates downstream functionalization. This electron-deficient aromatic scaffold integrates readily into pharmaceutical intermediates and bioactive molecule frameworks under standard conditions.
3-Fluoro-4-formylbenzoic acid serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The ortho-fluoro and para-formyl groups enable selective functionalization via nucleophilic substitution or condensation reactions, while the carboxylic acid facilitates derivatization through esterification, amide coupling, or salt formation. Its bench-stable crystalline form and compatibility with standard reaction conditions make it well-suited for scalable medicinal chemistry campaigns.
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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: