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Structure of 21622-01-5
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Ethyl cyclopent-3-enecarboxylate features a conjugated enoate system with a rigid cyclopentene backbone, enabling efficient Diels-Alder cycloadditions. The ester functionality provides stability and facilitates downstream transformations. This reagent integrates readily into complex molecular architectures under mild conditions.
Ethyl cyclopent-3-enecarboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted cyclopentane derivatives via Diels-Alder reactions and conjugate additions. Its enone functionality supports broad functional group tolerance and facilitates downstream transformations such as hydrogenation and electrophilic functionalization. The compound exhibits excellent bench stability and is readily purified by standard chromatographic methods, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS02
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Signal Word : Danger
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UN#: 3272
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Class : 3
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Packing Group : Ⅱ
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Hazard Statements : H225
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: