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Structure of 3901-07-3
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(E)-Methyl 4-methoxycinnamate features a conjugated trans-alkene system flanked by an electron-rich methoxy group and a polar ester moiety, enabling efficient incorporation into photoreactive frameworks. This bench-stable compound integrates readily into synthetic routes requiring extended π-conjugation or controlled reactivity under standard conditions.
(E)-Methyl 4-methoxycinnamate serves as a versatile synthetic intermediate for the construction of styryl-containing architectures. Its conjugated enoate system enables reliable Michael additions, Diels–Alder cycloadditions, and palladium-catalyzed cross-coupling reactions. The methyl ester and para-methoxy substituent provide excellent stability, solubility in common organic solvents, and compatibility with diverse functional groups, facilitating straightforward purification and integration into multi-step syntheses.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: