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Structure of 15191-36-3
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2-Bromo-4,6-dimethylphenol features a bromine substituent at the ortho position relative to the phenolic hydroxyl, combined with methyl groups at the 4- and 6-positions. This substitution pattern imparts enhanced stability and steric shielding around the reactive site. The compound serves as a selective electrophilic reagent in aromatic coupling reactions, particularly in the synthesis of functionalized heterocycles and advanced intermediates for agrochemicals and pharmaceuticals.
2-Bromo-4,6-dimethylphenol serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted aromatic systems via palladium-catalyzed cross-coupling reactions. Its bromine substituent exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the ortho-methyl groups provide steric protection and enhance bench stability. The phenolic hydroxyl group allows for selective derivatization, facilitating the construction of functionalized heterocycles and complex scaffolds relevant to medicinal chemistry and materials science.
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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: