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Structure of 20432-35-3
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This (E)-configured acrylaldehyde features a para-dimethylaminophenyl group, delivering strong electron donation and enhanced conjugation. The aldehyde functionality enables direct participation in condensation reactions, Michael additions, and imine formation. This compound exhibits high reactivity under mild conditions and maintains stability during standard bench handling.
(E)-3-(4-(Dimethylamino)phenyl)acrylaldehyde serves as a versatile building block in synthetic organic chemistry, enabling the construction of conjugated enone systems and heterocyclic scaffolds. Its well-defined (E)-configuration ensures stereochemical fidelity in Michael additions and condensation reactions. The aldehyde functionality facilitates efficient derivatization, while the dimethylamino group enhances electron density for improved reactivity in electrophilic substitutions. Bench-stable and readily purified by column chromatography, it functions effectively in multi-step syntheses targeting functionalized aromatic systems and pharmaceutical intermediates.
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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: