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Structure of 62708-42-3
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2-(Prop-2-en-1-yl)benzaldehyde features a conjugated enal system that enables efficient Michael additions and Diels-Alder reactions. The aldehyde group pairs with the electron-rich vinyl substituent to facilitate cascade cyclizations under mild conditions. This structure delivers high regioselectivity in heterocycle synthesis and serves as a key scaffold for bioactive molecule construction.
2-(Prop-2-en-1-yl)benzaldehyde serves as a versatile synthetic building block for constructing substituted stilbenes and functionalized aromatic systems. Its conjugated enal moiety enables efficient Michael additions, Diels–Alder cycloadditions, and palladium-catalyzed coupling reactions. The aldehyde functionality offers high reactivity in condensation processes, while the allyl group provides compatibility with standard cross-coupling protocols. Bench-stable and readily purified by distillation or chromatography, it functions effectively in multi-step syntheses of bioactive heterocycles 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-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: