β-Naphthol methyl ether
From Infogalactic: the planetary knowledge core
(Redirected from Nerolin)
Lua error in package.lua at line 80: module 'strict' not found.
 |
|
| Names | |
|---|---|
| IUPAC name
2-Methoxynaphthalene
|
|
| Other names
2-Naphthol methyl ether; 2-Naphthyl methyl ether; β-Methoxynaphthalene; β-Methyl naphthyl ether; β-Naphthol methyl ether; Nerolin; Yara yara
|
|
| Identifiers | |
| 93-04-9 | |
| ChemSpider | 6852 |
| Jmol 3D model | Interactive image |
| PubChem | 7119 |
|
|
|
|
| Properties | |
| C11H10O | |
| Molar mass | 158.20 g·mol−1 |
| Vapor pressure | {{{value}}} |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
| Infobox references | |
β-Naphthol methyl ether, also called 2-methoxynaphthalene or yara yara, [1] is a stabilizer found in gunpowder, particularly smokeless gunpowders. It is soluble in alcohol, and insoluble in water and dipropylene glycol.
Studies have also been done on the antiinflammatory effect of β-naphthol methyl ether[2] and on how it behaves in time-resolved resonance Raman studies.[3]
References
<templatestyles src="Reflist/styles.css" />
Cite error: Invalid <references> tag; parameter "group" is allowed only.
<references />, or <references group="..." /><templatestyles src="Asbox/styles.css"></templatestyles>
 |
This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
- ↑ "2-methoxynaphthalene", The Good Scents Company, 2012
- ↑ Cavrini V, Roveri P, Gatti R, Ferruzzi C, Panico AM, Pappalardo MS. "Synthesis of 2-methoxynaphthalene derivatives as potential anti-inflammatory agents", 2010
- ↑ Himansu Mohapatra and S. Umapathy, "Time-Resolved Resonance Raman Studies on Proton-Induced Electron-Transfer Reaction from Triplet Excited State of 2-Methoxynaphthalene to Decafluorobenzophenone", The Journal of Physical Chemistry, 2010
