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Structure of 64154-10-5
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This acrylate features a brominated furan ring that enables direct functionalization in cross-coupling reactions. The conjugated enoic acid moiety enhances reactivity in Michael additions and polymerization processes, offering a stable, moisture-tolerant handle for synthetic design.
3-(5-Bromofuran-2-yl)prop-2-enoic acid serves as a versatile building block for the synthesis of biologically relevant heterocycles and conjugated systems. Its structure combines a brominated furan moiety with an α,β-unsaturated carboxylic acid, enabling direct participation in palladium-catalyzed cross-coupling reactions and Michael additions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthetic sequences in medicinal chemistry and materials science applications.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: