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2,6-Dimethoxynaphthalene
  • Chemical Name: 2,6-Dimethoxynaphthalene
  • CAS No.: 5486-55-5

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1.What is the 2,6-Dimethoxynaphthalene ?

Used in Chemical Synthesis:
2,6-Dimethoxynaphthalene is used as an intermediate in the synthesis of various organic compounds and dyes. Its unique structure allows for the creation of a wide range of derivatives with diverse applications in the chemical industry.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,6-Dimethoxynaphthalene is studied for its potential antifungal and antimicrobial properties. Its ability to inhibit the growth of certain fungi and bacteria makes it a candidate for the development of new antimicrobial agents.
Used in Material Science:
2,6-Dimethoxynaphthalene is utilized in the development of optical and electronic materials due to its light-absorbing and fluorescent characteristics. These properties are beneficial for applications in areas such as sensors, displays, and photovoltaic devices.
Used in Research:
In the field of scientific research, 2,6-Dimethoxynaphthalene serves as a model compound for studying the effects of methoxy substitution on the physical and chemical properties of naphthalene derivatives. This helps in understanding the structure-property relationships and contributes to the advancement of material science and organic chemistry.

2.6-dihydroxynaphthalene
581-43-1

2.6-dihydroxynaphthalene

methyl iodide
74-88-4

methyl iodide

2,6-dimethoxylnaphthalene
5486-55-5,117119-43-4

2,6-dimethoxylnaphthalene

Conditions
Conditions Yield
With sodium hydride;
92%
With potassium carbonate; In N,N-dimethyl-formamide; at 85 ℃; for 3h;
85%
With potassium carbonate; In N,N-dimethyl-formamide; at 85 ℃; for 3h;
85%
2.6-dihydroxynaphthalene; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 0.5h;
methyl iodide; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; for 16h;
80%
2.6-dihydroxynaphthalene; With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 0.5h;
methyl iodide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 16h;
73%
With potassium carbonate; In N,N-dimethyl-formamide;
2.6-dihydroxynaphthalene
581-43-1

2.6-dihydroxynaphthalene

dimethyl sulfate
77-78-1

dimethyl sulfate

2,6-dimethoxylnaphthalene
5486-55-5,117119-43-4

2,6-dimethoxylnaphthalene

Conditions
Conditions Yield
2.6-dihydroxynaphthalene; With sodium hydride; In N,N-dimethyl-formamide; at -78 - 20 ℃; for 2h; Inert atmosphere;
dimethyl sulfate; at -78 - 20 ℃;
85.1%
With methanol; sodium hydroxide;
With sodium hydroxide; 1.) 55 deg C, 2 h, 2.) reflux 2 h;
With sodium hydroxide;

2.What is the CAS number for 2,6-Dimethoxynaphthalene ?

The CAS number of 2,6-Dimethoxynaphthalene is 5486-55-5.

More information of 2,6-Dimethoxynaphthalene 5486-55-5 are:

CAS?Number

5486-55-5

Density

1.097 g/cm3

Melting Point

152.5-153.5 ºC

Boiling Point

311.2 °C at 760 mmHg

Flash Point

130.3 °C

Vapor Pressure

5.02E-11mmHg at 25°C

Refractive Index

1.736

HS CODE

2909309090

PSA

18.46000

LogP

2.85700

3.What are another words for 2,6-Dimethoxynaphthalene ?

Synonyms?for?2,6-Dimethoxynaphthalene 5486-55-5:2,6dimethoxylNaphthalene

4.What is the molecular formula of 2,6-Dimethoxynaphthalene?

The chemical formula of ?2,6-Dimethoxynaphthalene is?C12H12O2 which containing 12 Carbon atoms,12 Hydrogen atoms and 2 Oxygen atoms,and the molecular weight of??2,6-Dimethoxynaphthalene?is 188.226.

5.What is 2,6-Dimethoxynaphthalene (5486-55-5) used for?

2,6-Dimethoxynaphthalene is a chemical compound characterized by the molecular formula C12H12O2. It is a naphthalene derivative featuring two methoxy groups attached at the 2 and 6 positions on the naphthalene ring. 2,6-Dimethoxynaphthalene is recognized for its light-absorbing and fluorescent properties, as well as its potential pharmaceutical properties, including antifungal and antimicrobial activities. It serves as a versatile intermediate in the synthesis of organic compounds and dyes, and is also valuable in the development of optical and electronic materials.

InChI:InChI=1/C17H10N2O2/c20-16-13-7-1-4-11-5-2-8-14(15(11)13)17(21)19(16)12-6-3-9-18-10-12/h1-10H

Relevant articles related to 2,6-Dimethoxynaphthalene:

Article

Source

A novel methoxy-decorated metal-organic framework exhibiting high acetylene and carbon dioxide storage capacities

Duan, Xing,Cui, Yuanjing,Yang, Yu,Qian, Guodong

, p. 1464 - 1469 (2017/03/17)

Comparative Evaluation of Substituent Effect on the Photochromic Properties of Spiropyrans and Spirooxazines

Balmond, Edward I.,Tautges, Brandon K.,Faulkner, Andrea L.,Or, Victor W.,Hodur, Blanka M.,Shaw, Jared T.,Louie, Angelique Y.

, p. 8744 - 8758 (2016/10/14)

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