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Structure of 98548-82-4
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4-(Dimethylamino)-2-butenoic acid features a conjugated enoic acid scaffold bearing a dimethylamino group that enhances electron density at the β-position. This structural motif enables facile participation in Michael additions and facilitates coupling reactions under mild conditions. The molecule exhibits improved solubility in polar organic solvents, supporting its use in synthetic peptide modifications and bioconjugation workflows.
4-(Dimethylamino)-2-butenoic acid serves as a versatile building block for synthesizing bioactive heterocycles and functionalized alkenes. Its conjugated enoic acid moiety enables reliable Michael additions, Diels-Alder reactions, and palladium-catalyzed couplings. The dimethylamino group enhances electron density for nucleophilic transformations while maintaining bench stability and compatibility with common protecting groups. This compound facilitates efficient access to substituted pyrrolidines and other nitrogen-containing scaffolds relevant to medicinal chemistry 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-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: