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Structure of 18113-03-6
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2-Chloro-4-methoxyphenol offers a strategic combination of electron-donating and halogenated functionality, enabling efficient coupling in cross-coupling and Ullmann-type reactions. The para-methoxy group enhances solubility and stabilizes reaction intermediates, while the ortho-chlorine serves as a direct handle for palladium-catalyzed transformations. This phenolic scaffold integrates readily into bioactive molecule design, particularly in agrochemical and pharmaceutical synthesis pathways.
2-Chloro-4-methoxyphenol serves as a versatile intermediate in the synthesis of pharmaceuticals and agrochemicals, enabling efficient functionalization via palladium-catalyzed cross-coupling reactions. Its ortho-chloro and para-methoxy substituents provide orthogonal reactivity for selective transformations, while the phenolic hydroxyl group allows for derivatization or protection. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for scalable synthetic processes.
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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: