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Structure of 76649-16-6
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Ethyl trans-4-decenoate features a conjugated enoate system that enables efficient participation in [3+2] cycloadditions and Diels-Alder reactions. This trans-configured ester delivers high stereoselectivity in synthetic transformations, serving as a robust scaffold for complex molecular architectures. The ethyl ester group enhances solubility and stability under standard conditions.
Ethyl trans-4-decenoate serves as a versatile linear unsaturated ester scaffold for transition-metal-catalyzed cross-coupling and conjugate addition reactions. Its well-defined trans-alkene geometry enables stereoselective transformations, while the terminal olefin and ester functionalities offer orthogonal reactivity for downstream functionalization. The compound exhibits excellent bench stability and is readily purified by standard distillation or chromatography, facilitating integration into complex molecule synthesis workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: