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Structure of 38678-86-3
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2-Bromo-4-ethylaniline features a bromine atom at the ortho position relative to the amino group, enhancing electrophilic reactivity in coupling reactions. The para-ethyl substituent imparts moderate electron-donating character and improves solubility in organic media. This arylamine derivative serves as a key intermediate in the synthesis of pharmaceuticals and functional dyes, offering stable handling under standard bench conditions.
2-Bromo-4-ethylaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aniline nitrogen and ortho-position. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the ethyl group provides steric and electronic modulation. The compound exhibits good bench stability and compatibility with standard purification techniques, making it suitable for iterative synthetic workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: