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Structure of 1378875-92-3
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Methyl 3-bromo-2,6-difluorobenzoate features a trifunctional aromatic core with strategically positioned bromo and difluoro substituents that enable selective cross-coupling reactions. The ester group provides synthetic versatility for downstream derivatization, while the electron-deficient ring enhances reactivity in palladium-catalyzed transformations. This bench-stable compound serves as a key intermediate in pharmaceutical and agrochemical synthesis.
Methyl 3-bromo-2,6-difluorobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The ortho-fluoro substituents enhance electrophilicity at the adjacent carbon, facilitating nucleophilic aromatic substitution under mild conditions. Bench-stable and readily purified by column chromatography, it functions as a key intermediate for constructing complex fluorinated heterocycles and bioactive scaffolds.
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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-H320-H335
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: