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Structure of 60811-17-8
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5-Bromo-2-chloroaniline features a bromine substituent at the 5-position and a chlorine atom at the 2-position of the aniline ring, delivering enhanced electron-withdrawing character. This ortho-halogenated scaffold enables selective coupling reactions in pharmaceutical synthesis and serves as a key intermediate for functionalized aromatic systems under standard conditions.
5-Bromo-2-chloroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aromatic ring through palladium-catalyzed cross-coupling reactions. Its dual halogenation pattern supports sequential transformations with high regiocontrol, while the primary amine facilitates derivatization via acylation, sulfonation, or reductive amination. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses requiring orthogonal reactivity.
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302+H312-H315-H319-H331-H335
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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: