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Structure of 5473-01-8
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2-Bromo-6-methoxyaniline features a bromine substituent at the ortho position relative to the amino group and a methoxy group at the para position, creating a uniquely activated aromatic scaffold. This electron-rich framework facilitates efficient coupling reactions in cross-coupling and Ullmann-type transformations. The compound exhibits excellent bench stability and solubility in common organic solvents, enabling straightforward integration into synthetic workflows for pharmaceutical intermediates and functional materials.
2-Bromo-6-methoxyaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted anilines via Pd-catalyzed cross-coupling reactions. Its bromo group facilitates reliable C–C bond formation under standard Suzuki, Stille, or Negishi conditions, while the methoxy substituent provides moderate electron donation and enhanced solubility. The compound exhibits good bench stability and is readily purified by recrystallization, supporting scalable synthesis workflows.
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GHS Pictogram :
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GHS No : GHS07,GHS09
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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-H317-H411
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Precautionary Statements : P261-P264-P270-P272-P273-P280-P302+P352-P363-P391-P501
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Lot numbers can be found on the outside label of a product: