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Structure of 26050-64-6
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Methyl 4-bromo-3,5-dimethoxybenzoate features a brominated aromatic core flanked by two methoxy groups, delivering enhanced electron density and stability. This bench-stable reagent integrates readily into Suzuki-Miyaura couplings and serves as a key intermediate in the synthesis of bioactive heterocycles and functionalized pharmaceuticals.
Methyl 4-bromo-3,5-dimethoxybenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its bromine substituent enables efficient palladium-catalyzed cross-coupling reactions, while the ortho-dimethoxy groups provide steric and electronic modulation. The methyl ester functionality facilitates further transformations, including hydrolysis or reduction. Bench-stable and readily purified by column chromatography, it functions reliably in standard synthetic 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: