Basic information Safety Supplier Related

2,5-Dimethoxynaphthalene

Basic information Safety Supplier Related

2,5-Dimethoxynaphthalene Basic information

Product Name:
2,5-Dimethoxynaphthalene
Synonyms:
  • 1,6-DIMETHOXYNAPHTHALENE, 98+%
  • 2,5(1,6)-Dimethoxy Naphthalene
  • 1,6-DimethoxylNaphthalene
  • 1,6-DIMETHOXYNAPHTHALENE
  • 2,5-DIMETHOXY NAPHTHALENE
  • 3,8-DiMethoxynaphthalene
  • NSC 167477
  • Naphthalene, 1,6-diMethoxy-
CAS:
3900-49-0
MF:
C12H12O2
MW:
188.22
Product Categories:
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Aromatics
  • Intermediates
  • Intermediates of Dyes and Pigments
  • FINE Chemical & INTERMEDIATES
  • Naphthalene derivatives
Mol File:
3900-49-0.mol
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2,5-Dimethoxynaphthalene Chemical Properties

Melting point:
56-60 °C(lit.)
Boiling point:
123°C 0,8mm
Density 
1.097±0.06 g/cm3(Predicted)
Flash point:
123°C/0.8mm
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform, Dichloromethane
form 
Solid
color 
Brown
BRN 
1945987
CAS DataBase Reference
3900-49-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
41
Safety Statements 
26-36/39
WGK Germany 
3
HS Code 
2909309090

MSDS

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2,5-Dimethoxynaphthalene Usage And Synthesis

Chemical Properties

Brown Solid

Uses

Intermediate in the production of tetralin derivatives

Synthesis

575-44-0

74-88-4

3900-49-0

In a round-bottomed flask equipped with a magnetic stirrer, 1.6 g (10.0 mmol) of 1,6-dihydroxynaphthalene (compound 39, purchased from Tokyo Chemical Industry Co., Ltd.) was dissolved in 15 mL of N,N-dimethylformamide (DMF). Subsequently, 14.2 g (100.0 mmol) of iodomethane (purchased from Wako Pure Chemical Industries, Ltd.) and 13.8 g (100.0 mmol) of potassium carbonate (purchased from Wako Pure Chemical Industries, Ltd.) were added to the solution. The reaction mixture was stirred at room temperature for 2 hours. After completion of the reaction, the reaction mixture was extracted by adding dichloromethane and water to the reaction mixture and the organic layer was separated and washed with distilled water. The solvent was removed by distillation under reduced pressure to give 1.7 g (yield: 90%) of 2,5-dimethoxynaphthalene (compound 40) as a colorless liquid.

References

[1] Patent: US2017/342031, 2017, A1. Location in patent: Paragraph 0643

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