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Structure of 93839-14-6
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2,4-Dichloro-6-methoxyaniline features a methoxy group at the para position relative to the amino functionality, enhancing solubility and modulating electronic effects. The ortho-chlorine substituents impart steric and electronic stabilization, enabling reliable coupling in pharmaceutical synthesis. This bench-stable derivative serves as a key intermediate in constructing bioactive heterocycles under standard conditions.
2,4-Dichloro-6-methoxyaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of heterocyclic scaffolds via coupling reactions. Its ortho-chloro substituents facilitate palladium-catalyzed cross-couplings, while the methoxy group offers moderate electronic modulation and enhanced solubility. The compound exhibits good bench stability and is compatible with standard functional group manipulations, supporting scalable synthesis workflows.
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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: