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Structure of 862728-59-4
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2-Cyclopropoxyethyl 4-methylbenzenesulfonate serves as a robust, bench-stable sulfonate ester for nucleophilic substitution reactions. The cyclopropoxy ether moiety enhances solubility and stability, while the para-methyl group modulates electronic properties. This reagent facilitates efficient coupling in synthetic workflows requiring mild activation conditions.
2-Cyclopropoxyethyl 4-methylbenzenesulfonate serves as a robust, bench-stable sulfonate ester for nucleophilic substitution reactions. It functions as an effective leaving group in SN2 transformations, enabling efficient functionalization of alcohols and amines under mild conditions. Its compatibility with diverse nucleophiles and ease of purification make it a practical choice for building molecular complexity in synthetic workflows.
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GHS Pictogram :
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GHS No : GHS06,GHS08
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Signal Word : Danger
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UN#: 2810
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331-H341
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: