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Structure of 710-43-0
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cis-Diethyl cyclopropane-1,2-dicarboxylate features a rigid, strained cyclopropane ring with adjacent ester groups, enabling precise stereochemical control in cycloaddition reactions. The cis configuration imparts defined spatial orientation, facilitating its use in asymmetric synthesis and natural product derivatization. This bench-stable compound integrates readily into complex molecular architectures under standard conditions.
cis-Diethyl cyclopropane-1,2-dicarboxylate serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective transformations via its strained cyclopropyl ring. The molecule facilitates efficient ring-opening reactions and functions as a key intermediate in the synthesis of bioactive heterocycles and natural product analogs. Its bench-stable nature and compatibility with common functional groups support reliable handling and purification in multi-step sequences.
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Lot numbers can be found on the outside label of a product: