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Structure of 65262-96-6
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3-Chloro-5-methoxyphenol features a phenolic hydroxyl group flanked by electron-withdrawing chlorine and electron-donating methoxy substituents, creating a uniquely polarized aromatic system. This structural motif enables direct participation in cross-coupling reactions and facilitates incorporation into bioactive scaffolds requiring balanced electronic properties. The compound exhibits enhanced solubility in organic solvents compared to unsubstituted phenols and maintains stability under standard bench conditions.
3-Chloro-5-methoxyphenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to functionalized aromatic scaffolds. Its ortho-chloro and para-methoxy substituents provide predictable reactivity in palladium-catalyzed cross-coupling reactions and allow for selective derivatization via electrophilic substitution or nucleophilic displacement. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic campaigns requiring reliable functional group compatibility.
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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: