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Structure of 5400-76-0
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2,4,6-Trichloro-3-methylaniline features a sterically hindered aromatic core with electron-deficient chlorine substituents and a methyl group at the 3-position, enabling selective coupling reactions in pharmaceutical intermediates. This bench-stable derivative integrates readily into complex molecular architectures under mild conditions.
2,4,6-Trichloro-3-methylaniline serves as a valuable building block for the synthesis of heterocyclic compounds and functionalized aromatic systems. Its three chlorine substituents enable efficient electrophilic substitution and palladium-catalyzed coupling reactions, while the methyl group enhances solubility and modulates electronic effects. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic workflows in medicinal chemistry and agrochemical development.
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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: