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Structure of 23051-44-7
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This malononitrile derivative features a sterically hindered cyclohexenylidene core that enhances stability and facilitates efficient Michael additions. The electron-deficient double bond enables rapid conjugate addition reactions, making it valuable for synthesizing complex heterocycles under mild conditions.
2-(3,5,5-Trimethylcyclohex-2-en-1-ylidene)malononitrile serves as a versatile Michael acceptor and Diels-Alder dienophile, leveraging its conjugated enone-like system for efficient cycloaddition and nucleophilic addition reactions. Its sterically shielded cyclohexenylidene core enhances bench stability and simplifies purification, while the dual nitrile groups provide high reactivity in heterocycle synthesis and functional group interconversions.
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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 : H317
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Precautionary Statements : P261-P272-P280-P302+P352-P363-P501
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Lot numbers can be found on the outside label of a product: