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Structure of 10272-06-7
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3-Chloro-5-methoxyaniline features a chlorinated aromatic ring paired with electron-donating methoxy and amino groups, enabling selective coupling in pharmaceutical intermediates. This bench-stable derivative offers enhanced solubility and reactivity in amine-directed transformations under standard conditions.
3-Chloro-5-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 and meta-methoxy substituents provide predictable regioselectivity and enhanced functional group tolerance, facilitating downstream derivatization. The compound exhibits excellent bench stability and ease of purification, making it well-suited for high-throughput screening campaigns and process-scale applications.
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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: