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Structure of 58101-60-3
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Methyl cyclopent-3-ene-1-carboxylate features a conjugated enone system within a strained cyclopentane framework, enabling efficient Diels-Alder cycloadditions. The ester group provides a handle for selective derivatization, while the rigid, electron-deficient alkene enhances reactivity in [4+2] processes under mild conditions.
Methyl cyclopent-3-ene-1-carboxylate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized cyclopentane scaffolds. Its conjugated enone system facilitates Michael additions, Diels-Alder reactions, and transition-metal-catalyzed couplings. The ester group provides a handle for selective transformations, while the inherent ring strain supports controlled functionalization. Bench-stable and amenable to purification by distillation or chromatography, it functions reliably in multi-step syntheses of natural products and pharmaceutical intermediates.
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GHS Pictogram :
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GHS No : GHS02,GHS05
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅲ
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Hazard Statements : H226-H318
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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: