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Structure of 42392-68-7
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Diethyl 2-cyclopropylmalonate features a cyclopropyl-substituted malonate core, delivering high reactivity in enolate-mediated C–C bond formations. The strained cyclopropyl ring enhances electrophilic character at the α-position, enabling efficient alkylation under mild conditions. This bench-stable derivative integrates readily into complex molecule synthesis, particularly in stereoselective routes to functionalized cyclic scaffolds.
Diethyl 2-cyclopropylmalonate serves as a versatile building block in synthetic organic chemistry, enabling the efficient construction of cyclopropyl-substituted carboxylic acid derivatives. Its malonate functionality facilitates facile alkylation and decarboxylation sequences, providing access to valuable synthons for medicinal chemistry and natural product synthesis. The cyclopropyl group imparts unique stereochemical and conformational constraints, enhancing its utility in targeted molecular design. The compound exhibits good bench stability and is amenable to standard purification protocols, making it well-suited for routine laboratory use.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: