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Structure of 13330-65-9
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2,4-Dimethoxyphenol features two methoxy groups at the 2- and 4-positions of the phenolic ring, enhancing solubility and stability. This electron-rich scaffold serves as a key intermediate in synthesizing bioactive molecules and functional polymers. The para-methoxy substitution pattern imparts strong resonance stabilization to the phenoxide anion, enabling controlled reactivity in electrophilic coupling reactions.
2,4-Dimethoxyphenol serves as a versatile building block in synthetic organic chemistry, enabling the construction of bioactive heterocycles and pharmaceutical intermediates. Its ortho- and para-dimethoxy substitution pattern provides enhanced stability and facilitates electrophilic aromatic substitution reactions. The phenolic functionality allows for straightforward derivatization via etherification or coupling protocols, while the methoxy groups offer predictable regioselectivity and functional group tolerance in multistep syntheses.
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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: