Oxetene
(Redirected from Oxete)
<templatestyles src="Chembox/styles.css"/>
Template:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox Datapage checkTemplate:Chembox Footer| Template:Longitem | Template:Unbulleted list |
| Template:Longitem | 4652799 |
| ChEBI | Template:Unbulleted list |
| ChemSpider | Template:Unbulleted list |
| DrugBank | Template:Unbulleted list |
| EC Number | Template:Unbulleted list |
| KEGG | Template:Unbulleted list |
| Template:Longitem | Template:Unbulleted list |
| RTECS number | Template:Unbulleted list |
| Script error: No such module "collapsible list". | |
| Script error: No such module "collapsible list". | |
| Template:Longitem | C3H4O |
| Molar mass | 56.06326 |
Template:Chembox Footer/trackingScript error: No such module "TemplatePar".Template:Short description
Oxetene is an unsaturated heterocycle. The compound is unstableScript error: No such module "Unsubst". and has been synthesized.[1] Compared to oxetane, the saturated compound, oxetene is destabilized because the double bond increases the ring strain.Script error: No such module "Unsubst". Synthesis of some substituted derivatives has been reported.[2][3]
Oxetene is less studied than oxetane, a related compound that is the base of a number of organic molecules.[2]
Synthesis
Oxetene can be synthesised by the photochemical cyclization of acrolein:[4]