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Structure of 635-22-3
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4-Chloro-3-nitroaniline features a chlorinated aryl ring paired with adjacent nitro and amino groups, creating a versatile scaffold for pharmaceutical intermediates. The electron-deficient aromatic core enables efficient coupling reactions, while the ortho-nitro group enhances reactivity in transition-metal-catalyzed transformations. This compound demonstrates robust stability under standard handling conditions.
4-Chloro-3-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation into heterocyclic scaffolds via nucleophilic substitution or subsequent reduction. Its ortho-chloro and meta-nitro groups provide complementary reactivity for sequential functionalization, with the nitro group readily reduced to an amine under standard conditions. Bench-stable and compatible with common purification methods, it facilitates efficient access to substituted anilines and complex molecular architectures.
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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#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H300+H310+H330-H315-H319-H373-H411
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Precautionary Statements : P260-P262-P264-P270-P271-P273-P280-P284-P302+P352-P304+P340-P330-P361-P391-P405-P501
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Lot numbers can be found on the outside label of a product: