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Structure of 5211-02-9
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3-Chloro-4-ethoxyaniline features a chlorinated aromatic ring paired with an ethoxy substituent, delivering enhanced solubility and electronic modulation. This combination enables efficient incorporation into pharmaceutical intermediates and functional materials. The molecule exhibits bench-stable handling under standard conditions and serves as a key scaffold for coupling reactions in synthetic workflows.
3-Chloro-4-ethoxyaniline 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 ethoxy substituent enhances solubility and modulates electronic properties. The compound exhibits good bench stability and is compatible with standard purification protocols, making it a practical choice for multi-step synthetic sequences.
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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: