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Structure of 158966-62-2
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2-Chloro-6-methoxyaniline features a chlorinated aromatic ring paired with a methoxy group, delivering enhanced solubility and stability under standard conditions. This electron-rich scaffold enables efficient coupling reactions in synthetic workflows. The para-chloro substitution facilitates selective functionalization, while the ortho-methoxy group provides steric and electronic modulation. This compound serves as a key intermediate in agrochemical and pharmaceutical synthesis.
2-Chloro-6-methoxyaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to substituted anilines via palladium-catalyzed cross-coupling reactions. Its ortho-chloro group facilitates selective functionalization, while the methoxy substituent provides moderate electron donation and enhances solubility. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for use in multi-step syntheses of heterocyclic scaffolds and API 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: