Methyl Cinnamate TCI C0360

Chemical Identity

Other names: Cinnamic Acid Methyl Ester · Methyl trans-3-Phenylacrylate · trans-3-Phenylacrylic Acid Methyl Ester
CAS No.: 103-26-4
PubChem: CID 637520·SID 87565492
Formula: C10H10O2
Molecular weight: 162.19 g/mol
Purity: >99.0%(GC)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl (E)-3-phenylprop-2-enoate
SMILES: COC(=O)C=CC1=CC=CC=C1
InChIKey: CCRCUPLGCSFEDV-BQYQJAHWSA-N
MDL: MDL00008458

Rp 582.750,00

~~Rp 423.150,00~~ Rp 582.750,00

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Berat 25g

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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.

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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 Research doi: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 Communications doi:10.1080/00397919608003584
BANIK (2004). Samarium-induced reductive dimerization of methyl cinnamate: synthesis of 2,8-diamino chrysene. Tetrahedron Letters doi: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.