| 词条 | 2,5-Dihydroxycinnamic acid |
| 释义 |
| ImageFile = 2,5-Dihydroxycinnamic acid.svg | ImageSize = 200px | ImageAlt = Chemical structure of 2,5-dihydroxycinnamic acid | IUPACName = 3-(2,5-dihydroxyphenyl)prop-2-enoic acid | OtherNames = (2E)-3-(2,5-Dihydroxyphenyl)acrylic acid |Section1={{Chembox Identifiers | CASNo = 636-01-1 | ChemSpiderID = 6442618 | InChI = 1S/C9H8O4/c10-7-2-3-8(11)6(5-7)1-4-9(12)13/h1-5,10-11H,(H,12,13) | InChIKey = JXIPYOZBOMUUCA-UHFFFAOYSA-N | PubChem = 181581 | SMILES = C1=CC(=C(C=C1O)C=CC(=O)O)O |Section2={{Chembox Properties | C=9 | H=8 | O=4 | Appearance = | Density = | MeltingPt = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} 2,5-Dihydroxycinnamic acid is a hydroxycinnamic acid. It is an isomer of caffeic acid. Preparation2,5-Dihydroxycinnamic acid is produced by Elbs persulfate oxidation of o-Coumaric acid.[1][2] See also
References1. ^{{cite journal|last1=Cain|first1=J.C.|last2=Greenaway|first2=A.J.|title=Abstracts of Papers on Organic chemistry|journal=Journal of the Chemical Society, Abstracts|date=1907|volume=92|pages=A741-A812|doi=10.1039/CA9079200741|url=https://books.google.com/books?id=u19FAQAAIAAJ&pg=PA772#v=onepage&q&f=false}} {{Hydroxycinnamic acid}}{{DEFAULTSORT:Dihydroxycinnamic acid, 2,5-}}{{natural phenol-stub}}2. ^{{cite journal|last1=Otto|first1=Neubauer|last2=Flatow|first2=L.|title=Synthesen von Alkaptonsäuren|journal=Zeitschrift für Physiologische Chemie|date=1907|volume=52|pages=375–398|url=http://vlp.mpiwg-berlin.mpg.de/references?id=lit18540&page=p0375}} 2 : Hydroxycinnamic acids|Hydroquinones |
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