1,3-Dimethoxybenzene: Difference between revisions
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| Name = 1,3-Dimethoxybenzene |
| Name = 1,3-Dimethoxybenzene |
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| ImageFileL1 = 1,3-Dimethoxybenzene.svg |
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| ImageSizeL1 = 175 |
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| ImageFileR1 = 1,3-Dimethoxybenzene-3D-balls.png |
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| OtherNames = Dimethylresorcinol<br>Resorcinol dimethyl ether |
| OtherNames = Dimethylresorcinol<br>Resorcinol dimethyl ether |
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| IUPACName = 1,3-Dimethoxybenzene |
| IUPACName = 1,3-Dimethoxybenzene |
Latest revision as of 22:39, 1 April 2024
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Names | |||
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IUPAC name
1,3-Dimethoxybenzene
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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
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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).
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1,3-Dimethoxybenzene is an organic compound with the formula C6H4(OCH3)2. It is one of three isomers of dimethoxybenzene.
Uses[edit]
1,3-Dimethoxybenzene has been used in the synthesis of novel oxathiane spiroketal donors.[1]
Related compounds[edit]
References[edit]
- ^ 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.