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Structure of 61040-78-6
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This bench-stable, moisture-tolerant reagent features a trialkoxy-substituted phenyl core that enhances solubility in organic solvents. The primary alcohol functionality enables direct coupling or derivatization in synthetic workflows. Delivers high functional group compatibility for use in pharmaceutical intermediates and specialty polymers.
(2,4,6-Trimethoxyphenyl)methanol serves as a robust building block for aromatic scaffolds, leveraging its ortho/para-directing methoxy groups to facilitate electrophilic substitution and transition-metal-catalyzed coupling reactions. The benzylic alcohol functionality enables straightforward derivatization via oxidation, protection, or direct functionalization, while the trimethoxy pattern enhances solubility and stability under standard synthetic conditions. Its predictable reactivity profile makes it a practical choice for medicinal chemistry and materials 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 : P233-P260-P261-P264-P271-P280-P302+P352-P304+P340-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: