Names | |
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IUPAC name
1,3-Dimethoxybenzene | |
Other names
Dimethylresorcinol Resorcinol dimethyl ether | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.005.259 |
EC Number |
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PubChem CID |
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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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