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1,3-Dimethylimidazolium iodide

  • CasNo:4333-62-4

Product Description

Quality products?make an important contribution to long-term revenue and profitability. Top Quality Chinese Factory supply 4333-62-4 1,3-Dimethylimidazolium iodide

1.What is the 1,3-Dimethylimidazolium iodide ?

Used in Chemical Synthesis:
1,3-Dimethylimidazolium iodide is used as a reagent for chemical synthesis processes, particularly in the formation of new organic compounds. Its cationic nature allows it to participate in various reactions, facilitating the creation of a wide range of products.
Used in Pharmaceutical Industry:
1,3-Dimethylimidazolium iodide is used as a catalyst in the pharmaceutical industry for the synthesis of various drugs and active pharmaceutical ingredients. Its ability to facilitate reactions and improve reaction rates makes it a valuable tool in the development of new medications.
Used in Electrochemical Applications:
1,3-Dimethylimidazolium iodide is used as an electrolyte in electrochemical applications, such as in batteries and fuel cells. Its ionic nature and stability contribute to improved performance and efficiency in these energy storage and conversion systems.
Used in Material Science:
1,3-Dimethylimidazolium iodide is used as a component in the development of new materials, such as ionic liquids and polymers. Its unique properties can enhance the performance of these materials, making them suitable for various applications, including energy storage, separation processes, and environmental remediation.
Used in Analytical Chemistry:
1,3-Dimethylimidazolium iodide is used as an analytical reagent in various analytical techniques, such as chromatography and spectroscopy. Its ability to interact with different compounds and improve detection sensitivity makes it a valuable tool in the analysis of complex samples.

1,3-dimethyl-2-cyclohexyl-1-hydroxymethyl-1H-imidazolium iodide
111931-05-6

1,3-dimethyl-2-cyclohexyl-1-hydroxymethyl-1H-imidazolium iodide

1,3-dimethylimidazolim iodide
4333-62-4

1,3-dimethylimidazolim iodide

cyclohexanecarbaldehyde
2043-61-0

cyclohexanecarbaldehyde

Conditions
Conditions Yield
With sodium hydroxide; 6-aminohexanoic acid; In benzene;
1-methyl-1H-imidazole
616-47-7

1-methyl-1H-imidazole

methyl iodide
74-88-4

methyl iodide

1,3-dimethylimidazolim iodide
4333-62-4

1,3-dimethylimidazolim iodide

Conditions
Conditions Yield
In dichloromethane; for 1h;
100%
In dichloromethane; at 0 ℃; for 3h;
99%
at 60 ℃;
98%
In ethyl acetate; Reflux;
98.8%
In toluene; at 40 ℃; for 24h; Schlenk technique; Inert atmosphere;
98%
In ethyl acetate; Reflux;
98.8%
In acetonitrile; at 60 ℃; for 16h; Sealed tube;
98%
In ethyl acetate; at 20 ℃; for 48h;
98%
In toluene; at 50 ℃; Inert atmosphere;
97%
In toluene; for 12h; Reflux; Inert atmosphere;
97.1%
In dichloromethane; at 5 - 20 ℃; for 1h;
97%
In toluene; Reflux; Inert atmosphere;
97%
In benzene; for 5h; Heating;
94.2%
In dichloromethane; for 16h;
93%
In tetrahydrofuran; for 48h; Schlenk technique; Inert atmosphere; Reflux;
93.4%
In tetrahydrofuran; at 20 ℃; for 2h; Schlenk technique; Inert atmosphere;
93.4%
In ethyl acetate;
92%
In dichloromethane; at 0 ℃; for 4h;
92%
In acetonitrile; at 60 ℃; for 3h;
92%
at 20 ℃; for 72h;
91.2%
In toluene; at 20 ℃; for 12h; Inert atmosphere;
86%
In isopropyl alcohol; at 20 - 100 ℃; Inert atmosphere;
85%
In propan-1-ol; at 100 ℃; for 19h;
85%
In neat (no solvent); Inert atmosphere; Schlenk technique;
82%
In tetrahydrofuran; at 20 ℃; for 3h;
81%
In toluene; at 45 ℃; Sealed tube;
76.5%
In toluene; at 90 ℃;
75%
In tetrahydrofuran; at -0.16 ℃; for 1h; Inert atmosphere;
66%
In toluene; for 18h; Reflux;
65%
In tetrahydrofuran; for 24h; Inert atmosphere; Schlenk technique;
51%
In tetrahydrofuran; for 24h; Schlenk technique; Inert atmosphere; Reflux;
51%
In dichloromethane; at 20 ℃; for 16h;
45%
With diethyl ether;
In dichloromethane; Yield given; Ambient temperature;
In acetonitrile;
In acetonitrile; at 20 ℃; for 24h;
1-methyl-1H-imidazole; With sodium hydride; In tetrahydrofuran;
methyl iodide; In tetrahydrofuran; Further stages.;
In toluene; at 90 ℃; for 2h;
In diethyl ether;
In ethanol; Reflux;
at 85 ℃; for 48h; closed vessel;
In tert-butyl methyl ether; at 20 ℃;
In ethyl acetate;
at 20 ℃; for 6h;
In acetonitrile; at 0 ℃; for 1h;
In isopropyl alcohol; for 8h; Reflux;
In methanol; at 20 ℃; Cooling with acetone-dry ice;
In ethyl acetate; at 20 ℃; for 2h; Schlenk technique;
at 0 - 20 ℃; for 147h;
In dichloromethane; for 1h; Inert atmosphere;
In dichloromethane; for 1h;
at 20 ℃; for 2h;
In ethyl acetate; at 23 ℃; for 2h; Schlenk technique;
In acetonitrile; at 20 ℃; for 24h;
for 2.16667h; Inert atmosphere; Cooling with ice;
In dichloromethane; at 0 - 20 ℃; for 2h;
In dichloromethane; at 0 - 20 ℃; for 2.25h;
at 70 ℃; for 24h;
In ethanol; at 70 ℃;
In 1,1,1-trichloroethane; for 2.16h; Cooling with ice;
8.09 g
1-methyl-1H-imidazole; In dichloromethane; for 0.0833333h;
methyl iodide; In dichloromethane; at 20 ℃; for 16h;

2.What is the CAS number for 1,3-Dimethylimidazolium iodide ?

The CAS number of 1,3-Dimethylimidazolium iodide is 4333-62-4.

More information of 1,3-Dimethylimidazolium iodide 4333-62-4 are:

CAS?Number

4333-62-4

Melting Point

84.0 to 89.0 °C

HS CODE

29332900

PSA

8.81000

LogP

-3.14640

3.What are another words for 1,3-Dimethylimidazolium iodide ?

Synonyms?for?1,3-Dimethylimidazolium iodide 4333-62-4:1,3-Dimethylimidazoliumiodide (7CI);1H-Imidazolium, 1,3-dimethyl-, iodide (9CI);Imidazolium,1,3-dimethyl-, iodide (8CI);1,3-Dimethyl-1H-imidazolium iodide;1-Methylimidazole methiodide;N,N'-Dimethylimidazolium iodide;

4.What is the molecular formula of 1,3-Dimethylimidazolium iodide?

The chemical formula of ?1,3-Dimethylimidazolium iodide is?C5H9IN2 which containing 5 Carbon atoms,9 Hydrogen atoms,1 Iodine atoms and 2 Nitrogen atoms,and the molecular weight of??1,3-Dimethylimidazolium iodide?is 224.044.

5.What is 1,3-Dimethylimidazolium iodide (4333-62-4) used for?

1,3-Dimethylimidazolium iodide is an organic iodide salt characterized by its cationic component, 1,3-dimethylimidazolium. It is a compound with potential applications in various industries due to its unique properties.

InChI:InChI=1/C5H9N2/c1-6-3-4-7(2)5-6/h3-5H,1-2H3/q+1

Relevant articles related to 1,3-Dimethylimidazolium iodide:

Article

Source

Photochemical Reduction of CO2 Using 1,3-Dimethylimidazolylidene

Denning, Derek M.,Thum, Matthew D.,Falvey, Daniel E.

, p. 4152 - 4155 (2015)

Photochemistry of imidazolium cations. Water addition to methylimidazolium ring induced by UV radiation in aqueous solution

Sarmiento, Gabriela P.,Zelcer, Andrés,Espinosa, Mariela S.,Babay, Paola A.,Mirenda, Martin

, p. 155 - 163 (2016)

6.Buy 1,3-Dimethylimidazolium iodide with the best price .

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