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Description
Methyl Cinnamate (TCI C0360, CAS 103-26-4) is one of the most widely used cinnamate esters in synthetic and analytical laboratories. Its conjugated ester system enables hydrolysis, transesterification, conjugate addition, dihydroxylation, and epoxidation chemistry from a single compact building block. It also serves as a reference substrate in Heck coupling, cross-metathesis, and hydrogenation studies, and as a comparison standard in essential-oil analysis. AMI Scientific offers 25 g and 500 g packs supplied in original TCI packaging.
Scientific References
Singh et al. (1991). Changes in the Linalool and Methyl Cinnamate Amounts in a Methyl Cinnamate-rich Clone ofOcimum basilicumat Different Growth Stages. Journal of Essential Oil Researchdoi:10.1080/10412905.1991.9697993
Moyna et al. (1996). An Improved Procedure for the Epoxidation of Methyl Cinnamate Derivatives and Production of Acid Sensitive Epoxides. Synthetic Communicationsdoi:10.1080/00397919608003584
BANIK (2004). Samarium-induced reductive dimerization of methyl cinnamate: synthesis of 2,8-diamino chrysene. Tetrahedron Lettersdoi:10.1016/s0040-4039(04)00877-9
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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