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Structure of 84131-04-4
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This benzyloxy-functionalized sulfonate ester delivers a robust, moisture-tolerant leaving group for efficient etherification reactions. Featuring a triethylene glycol spacer flanked by benzyl-protected hydroxyls, it enables selective C–O bond formation under mild conditions. The electron-deficient para-methylphenylsulfonate moiety ensures high reactivity while maintaining stability during storage and handling.
2-(2-(2-(Benzyloxy)ethoxy)ethoxy)ethyl 4-methylbenzenesulfonate serves as a robust, bench-stable protecting group reagent for primary alcohols, enabling selective etherification under mild conditions. Its trifluoromethylsulfonate-like reactivity facilitates efficient glycosylation and oligosaccharide synthesis, with the benzyloxy chain providing orthogonal deprotection compatibility. The p-toluenesulfonate leaving group ensures high chemoselectivity in complex molecule assembly, while the extended polyether tether enhances solubility and reduces aggregation during purification.
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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: