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Names | |||
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IUPAC name 1,3-Dimethoxybenzene | |||
Other names
Dimethylresorcinol Resorcinol dimethyl ether | |||
Identifiers | |||
CAS Number | |||
3D model (JSmol) | |||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.005.259 | ||
EC Number |
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PubChem CID | |||
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CompTox Dashboard (EPA) | |||
InChI
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SMILES
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Properties | |||
Chemical formula | C8H10O2 | ||
Molar mass | 138.166 g·mol | ||
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 , 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.
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.