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Structure of 6283-25-6
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6-Chloro-3-nitroaniline features a chlorinated aromatic ring paired with electron-withdrawing nitro and amino groups, enabling selective coupling in heterocyclic synthesis. This bench-stable derivative integrates readily into pharmaceutical intermediates and advanced materials, offering predictable reactivity under standard conditions.
6-Chloro-3-nitroaniline serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, enabling efficient construction of substituted heterocycles. Its ortho-chloro and meta-nitro groups provide complementary reactivity for sequential functionalization, while the aniline core supports palladium-catalyzed couplings and nitro group reductions. Bench-stable and readily purified by recrystallization, it facilitates scalable, high-yield transformations in multi-step syntheses.
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GHS Pictogram :
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GHS No : GHS06,GHS08,GHS09
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Signal Word : Danger
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UN#: 2237
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H300-H310+H330-H373-H411
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Precautionary Statements : P260-P264-P273-P280-P284
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Lot numbers can be found on the outside label of a product: