2,5-Dihydroxycinnamic acid
Appearance
Names | |
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Preferred IUPAC name
(2E)-3-(2,5-Dihydroxyphenyl)prop-2-enoic acid | |
Other names
(2E)-3-(2,5-Dihydroxyphenyl)acrylic acid, grevillic acid
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Identifiers | |
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3D model (JSmol)
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ChemSpider | |
PubChem CID
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UNII | |
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Properties | |
C9H8O4 | |
Molar mass | 180.159 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2,5-Dihydroxycinnamic acid is a hydroxycinnamic acid derivative. It is an isomer of caffeic acid.
Preparation
[edit]2,5-Dihydroxycinnamic acid is produced by Elbs persulfate oxidation of o-coumaric acid.[1][2]
See also
[edit]References
[edit]- ^ Cain, J.C.; Greenaway, A.J. (1907). "Abstracts of Papers on Organic chemistry". Journal of the Chemical Society, Abstracts. 92: A741–A812. doi:10.1039/CA9079200741.
- ^ Otto, Neubauer; Flatow, L. (1907). "Synthesen von Alkaptonsäuren". Zeitschrift für Physiologische Chemie. 52 (3–4): 375–398. doi:10.1515/bchm2.1907.52.3-4.375.