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Structure of 36942-56-0
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3-Bromo-4-methylanisole features a bromine substituent at the meta position relative to the methoxy group, delivering enhanced reactivity in cross-coupling processes. The para-methyl group imparts steric and electronic modulation, improving selectivity in palladium-catalyzed transformations. This bench-stable aryl halide integrates seamlessly into complex molecule assembly under standard conditions.
3-Bromo-4-methylanisole serves as a versatile aryl building block in medicinal chemistry and process development, enabling palladium-catalyzed cross-coupling reactions such as Suzuki-Miyaura and Stille couplings. Its bromo group exhibits high reactivity under standard conditions, while the methoxy and methyl substituents provide orthogonal functionalization potential and enhanced solubility. The compound demonstrates excellent bench stability and is readily purified by distillation or column chromatography, facilitating integration into multi-step syntheses of bioactive heterocycles and pharmaceutical intermediates.
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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: