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Structure of 51806-20-3
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1,1-Diethoxy-2-iodoethane offers a stable, bench-ready platform for iodine-transfer reactions. The geminal diethoxy substitution enhances solubility and reduces hydrolytic sensitivity. This reagent facilitates efficient C–I bond formation under mild conditions, enabling direct functionalization in complex molecular scaffolds.
1,1-Diethoxy-2-iodoethane serves as a reliable electrophilic iodide source in transition-metal-catalyzed cross-coupling reactions, particularly in the synthesis of vinyl and aryl iodides. Its diethoxyacetyl scaffold enhances stability and solubility, enabling straightforward handling and purification. The molecule facilitates efficient C–I bond formation under mild conditions, supporting broad functional group tolerance and compatibility with common catalytic systems.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: