To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

Butin (molecule)

From Wikipedia, the free encyclopedia

Butin
Names
IUPAC name
(2S)-3′,4′,7-Trihydroxyflavan-4-one
Systematic IUPAC name
(2S)-2-(3,4-Dihydroxyphenyl)-7-hydroxy-4H-1-benzopyran-4-one
Other names
5-Deoxyeriodictyol
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • InChI=1S/C15H12O5/c16-9-2-3-10-12(18)7-14(20-15(10)6-9)8-1-4-11(17)13(19)5-8/h1-6,14,16-17,19H,7H2/t14-/m0/s1 checkY
    Key: MJBPUQUGJNAPAZ-AWEZNQCLSA-N checkY
  • InChI=1/C15H12O5/c16-9-2-3-10-12(18)7-14(20-15(10)6-9)8-1-4-11(17)13(19)5-8/h1-6,14,16-17,19H,7H2/t14-/m0/s1
    Key: MJBPUQUGJNAPAZ-AWEZNQCLBW
  • C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)OC1[C@H](OC2=C(C1=O)C=CC(=C2)O)C3=CC(=C(C=C3)O)O
  • O=C2c3c(O[C@H](c1ccc(O)c(O)c1)C2)cc(O)cc3
Properties
C15H12O5
Molar mass 272.256 g·mol−1
Density 1.485 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Butin is a flavanone, a type of flavonoid. The compound can be found in the seeds of Vernonia anthelmintica[1] (Asteraceae) and in the wood of Dalbergia odorifera[2] (Fabaceae).

Glycosides

References

  1. ^ Tian, G.; Zhang, U.; Zhang, T.; Yang, F.; Ito, Y. (2004). "Separation of flavonoids from the seeds of Vernonia anthelmintica Willd by high-speed counter-current chromatography". Journal of Chromatography A. 1049 (1–2): 219–222. doi:10.1016/S0021-9673(04)01276-2. PMID 15499936.
  2. ^ Liu, Rong-Xia; Wang, Qiao; Guo, Hong-Zhu; Li, Li; Bi, Kai-Shun; Guo, De-An (2005). "Simultaneous determination of 10 major flavonoids in Dalbergia odorifera by high performance liquid chromatography". Journal of Pharmaceutical and Biomedical Analysis. 39 (3–4): 469–476. doi:10.1016/j.jpba.2005.04.007. PMID 15935596.
  3. ^ Serbin, A. G; Borisov, M. I; Chernobai, V. T (1972). "Flavonoids of Bidens tripartita II". Chemistry of Natural Compounds. 8 (4): 439–441. doi:10.1007/BF00563663. S2CID 4813333.


Stub icon

This article about an aromatic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 7 April 2024, at 15:58
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy