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Thermo Scientific Chemicals
Methyl cinnamate, predominantly trans, 99%
CAS: 103-26-4 | C10H10O2 | 162.188 g/mol
化学物質識別子
CAS103-26-4
IUPAC Namemethyl (2E)-3-phenylprop-2-enoate
Molecular FormulaC10H10O2
InChI KeyCCRCUPLGCSFEDV-BQYQJAHWSA-N
SMILESCOC(=O)\C=C\C1=CC=CC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Colorless to white
FormFused solid
Assay (GC)≥98.5%
Melting Point (clear melt)32.0-39.0?C
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Suitable for battery materials development.
Applications
Methyl cinnamate was used to inhibit monophenolase and diphenolase activity of mushroom tyrosinase and it also has antimicrobial ability. It is mainly is used in the flavor and perfume industries. It is known to attract males of various orchid bees, such as Aglae caerulea.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
Methyl cinnamate was used to inhibit monophenolase and diphenolase activity of mushroom tyrosinase and it also has antimicrobial ability. It is mainly is used in the flavor and perfume industries. It is known to attract males of various orchid bees, such as Aglae caerulea.
Solubility
Insoluble in water.
Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Donald G.Lee; Udo A.Spitzer. The oxidation of methyl cinnamate by ruthenium tetroxide. J. Org. Chem. 1976, 41, (22),3644-3644
- Gerd Hallnemo; Christina Ullenius. Intramolecularly assisted addition of LiMe2 Cu to methyl cinnamates. Tetrahedron Letters. 1986, 27, (3),395-398