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2-Methoxynaphthalene

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2-Methoxynaphthalene
Names
Preferred IUPAC name 2-Methoxynaphthalene
Other names Methyl naphthalen-2-yl ether
Methyl 2-naphthyl ether
2-Naphthol methyl ether
2-Naphthyl methyl ether
β-Methoxynaphthalene
β-Methyl naphthyl ether
β-Naphthol methyl ether
Nerolin
Yara yara
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.002.013 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3Key: LUZDYPLAQQGJEA-UHFFFAOYSA-N
  • InChI=1/C11H10O/c1-12-11-7-6-9-4-2-3-5-10(9)8-11/h2-8H,1H3Key: LUZDYPLAQQGJEA-UHFFFAOYAR
SMILES
  • O(c2ccc1c(cccc1)c2)C
Properties
Chemical formula C11H10O
Molar mass 158.200 g·mol
Melting point 73–75 °C (163–167 °F; 346–348 K)
Boiling point 274 °C (525 °F; 547 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

2-Methoxynaphthalene, also called β-naphthol methyl ether or yara yara, 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 and on how it behaves in time-resolved resonance Raman studies.

Synthesis and uses

Nerolin can be prepared by alkylation of β-naphthol with dimethyl sulfate. It has a faint but persistent odor and used to be a scented compound found in soap and other products.

References

  1. ^ "CHAPTER P-6. Applications to Specific Classes of Compounds". Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 703. doi:10.1039/9781849733069-00648. ISBN 978-0-85404-182-4.
  2. "2-methoxynaphthalene", The Good Scents Company, 2012
  3. Cavrini V, Roveri P, Gatti R, Ferruzzi C, Panico AM, Pappalardo MS (1982). "Synthesis of 2-methoxynaphthalene derivatives as potential anti-inflammatory agents". Farmaco Sci (in Italian). 37 (3): 171–178. PMID 7067812.
  4. Mohapatra, Himansu; Umapathy, S. (2010). "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 A. 114 (47): 12447–12451. Bibcode:2010JPCA..11412447M. doi:10.1021/jp109821r. PMID 21058635.
  5. Mann, Frederick George (1952). Practical Organic Chemistry. Longmans, Green & Co. p. 175.
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