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Structure of 6085-92-3
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2-Chloro-N-methyl-4-nitroaniline features a chlorinated aromatic ring paired with a methylated aniline and a nitro group at the para position, enabling efficient coupling in cross-coupling reactions. The electron-deficient aryl chloride integrates readily into pharmaceutical intermediates and functional materials under standard conditions.
2-Chloro-N-methyl-4-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct introduction of both chloro and nitro functionalities adjacent to a methylamino group. Its reactivity facilitates nucleophilic aromatic substitution and subsequent coupling reactions, supporting the construction of complex heterocyclic scaffolds. Bench-stable and readily purified by crystallization, it offers reliable functional group tolerance in multi-step synthetic sequences.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: