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Structure of 5150-42-5
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2,3-Dimethoxyphenol features two methoxy groups positioned ortho to each other on a phenolic backbone, enhancing solubility and stabilizing the aromatic system. This configuration imparts strong electron-donating character, making it valuable in synthesis of complex natural products and functional materials. The compound exhibits bench-stable handling under standard conditions and integrates readily into oxidative coupling reactions.
2,3-Dimethoxyphenol serves as a valuable building block in synthetic organic chemistry, enabling access to substituted aromatic scaffolds via standard electrophilic and transition-metal-catalyzed coupling reactions. Its ortho-dimethoxy substitution pattern provides enhanced stability and facilitates selective functionalization, while the phenolic hydroxyl group allows for derivatization or protection under mild conditions. The compound’s bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for medicinal chemistry and natural product 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: