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Structure of 7686-78-4
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Diethyl 2-vinylcyclopropane-1,1-dicarboxylate features a strained cyclopropane ring flanked by two ester groups and a terminal vinyl moiety. This configuration enables participation in stereoselective cycloadditions and ring-opening reactions under mild conditions. The molecule exhibits enhanced stability compared to analogous systems due to electronic delocalization across the vinyl and ester functionalities, facilitating its use in complex synthetic sequences.
Diethyl 2-vinylcyclopropane-1,1-dicarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclopropanes and functionalized heterocycles. The vinyl group facilitates [2+2] cycloadditions and palladium-catalyzed couplings, while the geminal diester motif supports selective reduction and decarboxylation sequences. Its bench-stable nature and compatibility with diverse reaction conditions make it valuable for medicinal chemistry lead generation and complex molecule synthesis.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: