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Structure of 1001-75-8
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4-Methylpent-4-enoic acid features a conjugated enoic acid scaffold with a methyl-substituted double bond, offering enhanced stability and predictable reactivity in synthetic transformations. This electron-deficient alkene integrates readily into Michael addition cascades and serves as a key building block for bioactive heterocycles and functionalized polymers under standard conditions.
4-Methylpent-4-enoic acid serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized alkenyl and heterocyclic frameworks. Its conjugated enoic acid structure facilitates reliable Michael additions, Diels-Alder reactions, and palladium-catalyzed couplings. The methyl substituent enhances steric control and metabolic stability in downstream applications. Bench-stable and readily purified by recrystallization, it functions effectively in both small-molecule synthesis and medicinal chemistry campaigns requiring α,β-unsaturated carboxylic acid motifs.
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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: