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Structure of 20329-98-0
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This (E)-configured cinnamic acid derivative features three methoxy groups positioned at the 3,4,5-aryl ring sites, delivering enhanced electron density and solubility in organic solvents. The conjugated system enables efficient integration into photoreactive or bioconjugation scaffolds. Its bench-stable nature supports reliable use in synthetic workflows requiring precise functional group presentation.
(E)-3,4,5-Trimethoxycinnamic acid serves as a versatile building block in medicinal chemistry and natural product synthesis, offering a stable, bench-ready platform for structural diversification. Its conjugated enone system enables reliable Michael addition and palladium-catalyzed coupling reactions, while the three methoxy groups provide enhanced solubility and metabolic stability. The compound functions effectively in the construction of bioactive heterocycles and scaffold elaboration under standard reaction conditions.
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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: