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Structure of 760-58-7
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2-Cyano-4-methylpent-2-enoic acid features a conjugated enoic acid system flanked by a nitrile and methyl group, enabling efficient participation in Michael additions and cycloaddition reactions. This electron-deficient alkene integrates readily into synthetic scaffolds requiring high reactivity under mild conditions.
2-Cyano-4-methylpent-2-enoic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized heterocycles and bioactive scaffolds. Its conjugated enoate system facilitates Michael additions and Diels–Alder reactions, while the nitrile and carboxylic acid groups offer orthogonal handles for further derivatization. The compound exhibits good bench stability and is amenable to standard purification 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 : 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: