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Structure of 1564624-36-7
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Methyl 5-bromo-4-fluoro-2-methylbenzoate features a trifunctional aromatic core with strategically positioned bromo, fluoro, and methyl groups. This electron-deficient platform enables direct coupling in cross-coupling reactions, while the ester functionality offers synthetic versatility. The molecule exhibits robust stability under standard bench conditions and facilitates efficient derivatization in medicinal chemistry and materials synthesis workflows.
Methyl 5-bromo-4-fluoro-2-methylbenzoate serves as a versatile building block for late-stage functionalization in medicinal chemistry and agrochemical synthesis. Its orthogonal halogenation pattern enables selective cross-coupling reactions, particularly Pd-catalyzed Suzuki and Stille couplings, with high chemoselectivity. The methyl ester group provides a handle for further derivatization, while the fluorine and bromine substituents offer favorable electronic effects and metabolic stability. Bench-stable and readily purified by flash chromatography, it functions effectively in multi-step synthetic sequences requiring predictable reactivity and structural precision.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: