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Structure of 84646-68-4
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Methyl 1-(methoxycarbonyl)cyclopent-3-enecarboxylate features a conjugated enone system flanked by ester and cyclopentenyl moieties, enabling direct participation in Diels-Alder reactions. This strained, electron-deficient dienophile integrates efficiently into complex carbocyclic frameworks under mild conditions.
Methyl 1-(methoxycarbonyl)cyclopent-3-enecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclopentane scaffolds. The conjugated enoate system facilitates Michael additions and Diels-Alder reactions, while the ester group supports selective transformations under standard conditions. Its bench-stable nature and compatibility with diverse reaction protocols make it well-suited for medicinal chemistry and process development 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: