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| Names | |
|---|---|
| IUPAC name 1,3-Dimethoxybenzene | |
| Other names Dimethylresorcinol Resorcinol dimethyl ether | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.005.259 | 
| EC Number | 
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| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C8H10O2 | |
| Molar mass | 138.166 g·mol−1 | 
| Related compounds | |
| Related compounds | 1,2-Dimethoxybenzene; 1,4-Dimethoxybenzene | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
1,3-Dimethoxybenzene is an organic compound with the formula C6H4(OCH3)2. It is one of three isomers of dimethoxybenzene.
Uses
1,3-Dimethoxybenzene has been used in the synthesis of novel oxathiane spiroketal donors.[1]
Related compounds
References
- ↑ A. Fascione, Martin; J. Webb, Nicola; A. Kilner, Colin; L. Warriner, Stuart; Bruce Turnbull, W. (2011-12-28). "Stereoselective glycosylations using oxathiane spiroketal glycosyl donors". Merck. 348: 6–13. doi:10.1016/j.carres.2011.07.020. PMID 22200482.
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