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Structure of 2941-29-9
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Cyclopentanone-2-carbonitrile features a conjugated enone system paired with a nitrile group, enabling direct participation in Michael additions and nucleophilic transformations. The adjacent electron-withdrawing nitrile enhances electrophilicity at the β-position, facilitating efficient C–C bond formation under mild conditions. This versatile scaffold integrates readily into heterocyclic and bioactive molecule syntheses.
Cyclopentanone-2-carbonitrile serves as a versatile building block in synthetic organic chemistry, enabling efficient access to nitrogen-containing heterocycles and functionalized cyclopentane scaffolds. Its conjugated enone-nitrile system facilitates Michael additions, cyclizations, and transition-metal-catalyzed couplings. The molecule exhibits good bench stability and is readily purified by standard techniques, making it well-suited for iterative synthesis in 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: