1,2-Dimethoxybenzene
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Revision as of 05:10, 13 April 2010 by حسن علي البط (Talk) (Removed Category:Aromatic compounds (using HotCat))
1,2-Dimethoxybenzene | |
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1,2-Dimethoxybenzene | |
1,2-Dimethoxybenzene | |
Other names veratrole o-dimethoxybenzene pyrocatechol dimethyl ether | |
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers | |
CAS number | 91-16-7 |
ChemSpider | 6776 |
SMILES | Script error: No such module "collapsible list". |
style="background: #F8EABA; text-align: center;" colspan="2" | Properties | |
Molecular formula | C8H10O2 |
Molar mass | 138.16 g/mol |
Density | 1.084 g/cm³ |
Melting point |
22-23 °C |
Boiling point |
206-207 °C |
style="background: #F8EABA; text-align: center;" colspan="2" | Hazards | |
NFPA 704 | |
(what is this?) (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) | |
Infobox references |
1,2-Dimethoxybenzene, commonly known as veratrole, is a chemical compound with the formula C6H4(OCH3)2. It is the dimethyl ether derived from pyrocatechol. Veratrole is slightly soluble in water, but miscible in all organic solvents. It is a building block for the organic synthesis of other aromatic compounds. Veratrole is relatively electron-rich and thus readily undergoes electrophilic substitution.[1]
Related compounds
- 1,3-Dimethoxybenzene
- 1,4-Dimethoxybenzene
- Guaiacol, the monomethyl derivative of pyrocatechol
Literature
- Merck Index, 11th Edition, 9857.
References
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40px | This article about an aromatic compound is a stub. You can help ssf by expanding it. |
- ↑ Janssen, D. E.; Wilson, C. V. (1963), "4-Iodoveratrole", Org. Synth. ; Coll. Vol., 4: 547 Missing or empty
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