Dioxirane: Difference between revisions
Appearance
Content deleted Content added
m r2.5.2) (robot Adding: pl:Dioksiran |
Dioxirane.svg |
||
Line 1: | Line 1: | ||
{{chembox |
{{chembox |
||
|ImageFileL1=Dioxirane |
|ImageFileL1=Dioxirane.svg |
||
|ImageSizeL1=80px |
|ImageSizeL1=80px |
||
|ImageFileR1=Dioxirane-stick.png |
|ImageFileR1=Dioxirane-stick.png |
Revision as of 00:45, 6 February 2011
| |||
![]() | |||
Names | |||
---|---|---|---|
IUPAC name
Dioxirane
| |||
Identifiers | |||
3D model (JSmol)
|
|||
PubChem CID
|
|||
CompTox Dashboard (EPA)
|
|||
| |||
Properties | |||
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).
|
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] The only dioxirane in common use is dimethyldioxirane (DMDO), the oxirane derived from acetone.
See also
References
- ^ 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.
{{cite journal}}
: CS1 maint: multiple names: authors list (link)