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Structure of 46427-07-0
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(E)-2-Benzylidenesuccinic acid features a conjugated enone system stabilized by extended π-delocalization, enabling efficient participation in Diels-Alder cycloadditions. This bench-stable, crystalline reagent integrates readily into synthetic sequences requiring electron-deficient dienophiles.
(E)-2-Benzylidenesuccinic acid serves as a versatile diene in Diels-Alder reactions, enabling efficient access to substituted cyclohexene scaffolds. Its well-defined (E)-configuration ensures predictable stereochemistry, while the carboxylic acid functionalities facilitate downstream derivatization or salt formation. The compound exhibits good bench stability and is readily purified by recrystallization, making it suitable for routine synthetic workflows in organic and medicinal chemistry.
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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: