β-Naphthol methyl ether

From Infogalactic: the planetary knowledge core
(Redirected from Nerolin)
Jump to: navigation, search

Lua error in package.lua at line 80: module 'strict' not found.

β-Naphthol methyl ether
2-methoxynaphthalene.svg
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
  • InChI=1S/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3
    Key: LUZDYPLAQQGJEA-UHFFFAOYSA-N
  • InChI=1/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3
    Key: LUZDYPLAQQGJEA-UHFFFAOYAR
  • O(c2ccc1c(cccc1)c2)C
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

  1. "2-methoxynaphthalene", The Good Scents Company, 2012
  2. Cavrini V, Roveri P, Gatti R, Ferruzzi C, Panico AM, Pappalardo MS. "Synthesis of 2-methoxynaphthalene derivatives as potential anti-inflammatory agents", 2010
  3. 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


<templatestyles src="Asbox/styles.css"></templatestyles>