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Thermo Scientific Chemicals
Ethyl cinnamate, 98+%
CAS: 103-36-6 | C11H12O2 | 176.215 g/mol
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化學識別
CAS103-36-6
IUPAC Nameethyl (2E)-3-phenylprop-2-enoate
Molecular FormulaC11H12O2
InChI KeyKBEBGUQPQBELIU-CMDGGOBGSA-N
SMILESCCOC(=O)\C=C\C1=CC=CC=C1
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規格
規格表
規格表FormLiquid
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥98.0%
CommentMaterial Sourced in UK and US
Identification (FTIR)Conforms (UK Sourced Material)
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Ethyl cinnamate is used in medical intermediate, as a pharmaceutical intermediate and in organic synthesis.
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.
Applications
Ethyl cinnamate is used in medical intermediate, as a pharmaceutical intermediate and in organic synthesis.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, acids, bases and reducing agents.
Ethyl cinnamate is used in medical intermediate, as a pharmaceutical intermediate and in organic synthesis.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents, acids, bases and reducing agents.
RUO – Research Use Only
General References:
- 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).