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Structure of 69951-02-6
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2-Chloro-6-methyl-4-nitroaniline features a nitro group at the para position relative to the amino functionality, imparting strong electron-withdrawing character. The ortho-chloro and meta-methyl substituents provide steric and electronic modulation, enhancing stability under standard conditions. This aniline derivative serves as a key intermediate in the synthesis of dyes, agrochemicals, and pharmaceuticals, where its reactivity profile supports efficient coupling and functionalization.
2-Chloro-6-methyl-4-nitroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct substitution at the aromatic ring due to its complementary electron-withdrawing nitro group and activating chloro/methyl substituents. The molecule exhibits bench stability and facilitates straightforward functionalization via nucleophilic aromatic substitution or transition-metal-catalyzed coupling reactions. Its well-defined reactivity profile supports efficient access to complex heterocyclic scaffolds and drug-like intermediates.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: