Chemistry:2,5-Dihydroxycinnamic acid
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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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3D model (JSmol)
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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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Tracking categories (test):
2,5-Dihydroxycinnamic acid is a hydroxycinnamic acid. It is an isomer of caffeic acid.
Preparation
2,5-Dihydroxycinnamic acid is produced by Elbs persulfate oxidation of o-Coumaric acid.[1][2]
See also
References
- ↑ 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. https://books.google.com/books?id=u19FAQAAIAAJ&pg=PA772.
- ↑ 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. http://vlp.mpiwg-berlin.mpg.de/references?id=lit18540&page=p0375.
Original source: https://en.wikipedia.org/wiki/2,5-Dihydroxycinnamic acid.
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