Adverts

Open Access Articles- Top Results for Dioxirane

Dioxirane

Not to be confused with Dioxane.
#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. colspan=2 class="borderless" border=0 align=center #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.
Dioxirane

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

120px colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Names

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

IUPAC name
Dioxirane
colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Identifiers#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-



157-26-6 7pxY ChemSpider 396025 7pxN Jmol-3D images Image PubChem Template:Chembox PubChem/format colspan=2 style="background:#f8eaba; border-top:2px solid transparent; border-bottom:2px solid transparent; text-align:center;" #REDIRECTmw:Help:Magic words#Other
This page is a soft redirect. Properties

#REDIRECTmw:Help:Magic words#Other
This page is a soft redirect.-

CH2O2 Molar mass 46.03 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
 14pxN verify (what is10pxY/10pxN?) Infobox references

A dioxirane is a molecule containing a three-membered ring composed of one carbon and two oxygens. Somewhat unstable, they are used in organic synthesis as oxidizing reagents.[1] A dioxirane in common use is dimethyldioxirane (DMDO), the dioxirane derived from acetone.

See also

References

  1. ^ Ruggero Curci, Anna Dinoi, and Maria F. Rubino (1995). "Dioxirane oxidations: Taming the reactivity-selectivity principle" (PDF). Pure & Appl. Chem. 67 (5): 811–822. doi:10.1351/pac199567050811. 

Lua error in package.lua at line 80: module 'Module:Buffer' not found.