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Structure of 27960-21-0
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(E)-3-Methyl-2-hexenoic acid features a conjugated enoic acid scaffold with a methyl-substituted alkene, offering enhanced stability and defined stereochemistry. This bench-stable, moisture-tolerant reagent integrates readily into synthetic routes requiring geometrically pure α,β-unsaturated carboxylic acids for natural product synthesis and functional material design.
(E)-3-Methyl-2-hexenoic acid serves as a versatile building block for synthesizing α,β-unsaturated carboxylic acids and functionalized heterocycles. Its well-defined stereochemistry and conjugated enoic framework enable reliable participation in Michael additions, Diels–Alder reactions, and palladium-catalyzed couplings. The molecule exhibits good bench stability and facilitates straightforward purification via distillation or recrystallization, making it suitable 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: