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Structure of 56461-98-4
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2,6-Dichloro-4-methylaniline features a sterically hindered aromatic core with electron-withdrawing chlorine substituents flanking a methylaniline moiety. This configuration enhances regioselectivity in coupling reactions and provides improved stability under standard bench conditions. The compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals requiring halogenated aniline scaffolds.
2,6-Dichloro-4-methylaniline serves as a valuable building block in medicinal chemistry and agrochemical synthesis, offering a well-defined substitution pattern for directed ortho-metalation. Its trifunctional architecture enables selective functionalization at the 4-position while maintaining stability under standard reaction conditions. The compound facilitates efficient coupling reactions and heterocycle construction due to its favorable electronic profile and ease of purification.
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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: