I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Ethyl cinnamate is used in medical intermediate, as a pharmaceutical intermediate and in organic synthesis.
Caiding Xu.; Guoying Chen.; Chong Fu.; Xian Huang. The Wittig Reaction of Stable Ylide with Aldehyde Under Microwave Irradiation: Synthesis of Ethyl Cinnamates. Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry. 1995, 25 (15), 2229-2233.
P. L. Egerton.; E. M. Hyde.; J. Trigg.; A. Payne.; P. Beynon.; M. V. Mijovic.; A. Reiser. Photocycloaddition in liquid ethyl cinnamate and in ethyl cinnamate glasses. The photoreaction as a probe into the micromorphology of the solid. J. Am. Chem. Soc. 1981, 103 (13), 3859-3863.
Arylacrylic esters undergo reductive cross-coupling with alkylaldehydes, promoted by Mg in the presence of TMS chloride, giving 4-aryl-5-alkyl--butyrolactones in high yield: J. Org. Chem., 60, 458 (1995).
Gefahrenhinweise (EU): H303
May be harmful if swallowed.