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Structure of 1123-63-3
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4-Chloro-2,6-dimethylphenol features a chlorine substituent at the para position relative to the phenolic hydroxyl, flanked by two methyl groups that confer steric protection and enhance stability. This combination imparts high resistance to oxidation and facilitates handling under ambient conditions. The molecule serves as a key intermediate in agrochemical synthesis and functionalized aromatic building blocks for pharmaceutical development.
4-Chloro-2,6-dimethylphenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis. Its electron-rich aromatic core enables efficient electrophilic substitution and palladium-catalyzed coupling reactions. The chlorine atom provides a reliable handle for nucleophilic displacement, while the ortho-methyl groups enhance stability and influence regioselectivity. This compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for multi-step synthesis workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: