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
Languages
Recent
Show all languages
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

Methyl phenyl sulfoxide

From Wikipedia, the free encyclopedia

Methyl phenyl sulfoxide
Names
Preferred IUPAC name
(Methanesulfinyl)benzene
Other names
Methylsulfinylbenzene
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.013.438 Edit this at Wikidata
EC Number
  • 214-781-2
  • InChI=1S/C7H8OS/c1-9(8)7-5-3-2-4-6-7/h2-6H,1H3
    Key: JXTGICXCHWMCPM-UHFFFAOYSA-N
  • CS(=O)C1=CC=CC=C1
Properties
C7H8OS
Molar mass 140.20 g·mol−1
Appearance colorless or white solid
Density 1.19±0.1 g/cm3
Melting point 32 °C (90 °F; 305 K)
Boiling point 263.5 °C (506.3 °F; 536.6 K)
Hazards
GHS labelling:
GHS05: Corrosive
GHS07: Exclamation mark
Warning
H315, H318, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P310, P312, P321, P332+P313, P362, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Methyl phenyl sulfoxide is the organosulfur compound with the formula CH3S(O)C6H5. A low-melting white solid, it is an oxidized derivative of thioanisole.[1] The compound is a prototypical chiral sulfoxide. As such it has been prepared by asymmetric oxidation.[2]

References

  1. ^ Johnson, Carl R.; Keiser, Jeffrey E. (1966). "Methyl Phenyl Sulfoxide". Org. Syntheses. 46: 78. doi:10.15227/orgsyn.046.0078.
  2. ^ Kagan, Henri B.; Chellappan, Sheela K.; Lattanzi, Alessandra (2015). "(R)-(+)-Phenyl methyl sulfoxide". E-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rn00456. ISBN 978-0471936237.
This page was last edited on 28 April 2023, at 23:09
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