1,2-Butylene carbonate
<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 |
| 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 | Template:Chembox Elements/molecular formula |
| Molar mass | Template:Chem molar mass |
Template:Chembox Footer/trackingScript error: No such module "TemplatePar".Template:Short description
1,2-Butylene carbonate is an organic compound with formula Template:Chem/link, or (H5C2)(C2H3)(CO3). It is a double ester with the carbonate functional group bonded to both free ends of the 1,2-butylene group. It is also a heterocyclic compound with a five-membered ring, and can be seen as a derivative of dioxolane, specifically 4-ethyl-1,3-dioxolan-2-one.
1,2-Butylene carbonate is a polar aprotic solvent, which has been considered for electric battery applications (as a cheaper alternative to ionic liquids) and many other uses.[1]
See also
References
<templatestyles src="Reflist/styles.css" />
- ↑ Jacek Kumełan, Dirk Tuma, Sergey P. Verevkin and Gerd Maurer (2008), Solubility of Hydrogen in the Cyclic Alkylene Ester 1,2-Butylene Carbonate. J. Chem. Eng. Data, 2008, 53 (12), pp 2844–2850. Script error: No such module "CS1 identifiers"..
Script error: No such module "Check for unknown parameters".