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Structure of 216393-55-4
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3,5-Difluorobenzoic acid methyl ester features a fluorinated aromatic core with electron-withdrawing substituents that enhance reactivity in cross-coupling and functionalization processes. The methyl ester group provides stable, bench-ready handling while enabling straightforward hydrolysis or derivatization under standard conditions. This compound serves as a key building block for pharmaceutical intermediates and agrochemical scaffolds.
3,5-Difluorobenzoic acid methyl ester serves as a versatile building block in medicinal chemistry and synthetic organic chemistry. Its ortho-fluorinated aromatic core enables enhanced metabolic stability and modulates electronic properties in target molecules. The methyl ester group facilitates straightforward derivatization via hydrolysis or nucleophilic acyl substitution, while the difluoro substitution pattern supports predictable reactivity in coupling reactions and heterocycle formation. Bench-stable and easily purified, it functions effectively in standard synthetic workflows for API and agrochemical development.
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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-H319
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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: