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Structure of 6802-75-1
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Diethyl isopropylidenemalonate serves as a versatile synthon in asymmetric synthesis, featuring a stabilized enol ether moiety that enables selective Michael additions and cycloadditions. The electron-deficient double bond facilitates conjugate functionalization, while the isopropylidene group provides steric protection and enhanced shelf stability under standard conditions.
Diethyl isopropylidenemalonate serves as a versatile Michael acceptor and key building block in heterocyclic synthesis, enabling efficient access to substituted pyrrolidines and piperidines via cycloaddition or nucleophilic addition. Its stable enol ether functionality offers enhanced bench stability and compatibility with diverse reaction conditions, facilitating straightforward purification and scalability in medicinal chemistry 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 : 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: