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Structure of 96558-78-0
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3-Bromo-5-chlorophenylamine features a strategically positioned bromo and chloro substituent on the aromatic ring, enabling selective cross-coupling reactions. This electron-deficient aniline derivative offers enhanced reactivity in palladium-catalyzed transformations while maintaining bench-stable handling characteristics under standard conditions.
3-Bromo-5-chlorophenylamine serves as a versatile building block for the synthesis of pharmaceutical intermediates and functionalized heterocycles. Its ortho-halogenated arylamine framework enables palladium-catalyzed coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig amination, with high efficiency. The molecule exhibits excellent bench stability and compatibility with diverse functional groups, facilitating straightforward purification and integration into multi-step synthetic sequences.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2018
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Class : 6.1
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Packing Group : Ⅱ
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Hazard Statements : H301+H311+H331-H314
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Precautionary Statements : P260-P261-P264-P270-P271-P280-P301+P330+P331-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P330-P361+P364-P363-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: