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Structure of 6453-07-2
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Dimethyl 4-oxocyclopentane-1,2-dicarboxylate features a cyclopentane core bearing two ester groups and a ketone at the C4 position, enabling versatile reactivity in cycloadditions and ring-functionalization. The electron-deficient carbonyl enhances its utility in asymmetric synthesis, while the bench-stable diester moiety supports straightforward handling under standard conditions.
Dimethyl 4-oxocyclopentane-1,2-dicarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclopentane scaffolds. Its conjugated 1,2-dicarbonyl system facilitates nucleophilic additions and condensation reactions, while the ester groups support subsequent transformations such as hydrolysis, reduction, or cross-coupling. The molecule exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis in medicinal chemistry and natural product development.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: