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Structure of 72403-03-3
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2-Chloro-6-methoxyphenol offers a strategic combination of electron-withdrawing chlorine and electron-donating methoxy groups, enabling selective reactivity in electrophilic substitution. This balanced electronic profile supports its use as a key intermediate in agrochemical and pharmaceutical synthesis, where controlled functionalization is essential.
2-Chloro-6-methoxyphenol serves as a versatile building block in synthetic organic chemistry, enabling efficient construction of substituted aromatic scaffolds. Its ortho-chloro and para-methoxy functionalities offer complementary reactivity for palladium-catalyzed cross-coupling and electrophilic substitution reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development workflows requiring functional group tolerance and predictable regiochemistry.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: