Category: 1739-84-0

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. Application of C5H8N2.

Galvan, Vicente;Shrimant, Bharat;Bae, Chulsung;Prakash, G. K. Surya research published 《 Ionomer Significance in Alkaline Direct Methanol Fuel Cell to Achieve High Power with a Quarternized Poly(terphenylene) Membrane》, the research content is summarized as follows. Direct alk. fuel cells have recently shown a rapid surge in performance due to improvements to the anion exchange membrane (AEM) and electrocatalysts for oxygen reduction reaction (ORR). Recently, much focus has been in the area of improving the anion exchange ionomer (AEI), catalyst and AEM interface, mostly centered on the H₂/O₂ fuel cell. The use of liquids in fuel cells can offer some advantages compared to the H₂/O₂ fuel cell; thus, it is important to study the interaction between the AEI, catalyst and AEM in direct oxidation liquid fuel cells. This work reports the activity of the methanol oxidation reaction (MOR) in half-cell experiments with varying AEIs and the use of a poly(terphenylene) (TPN) membrane in an alk. direct methanol fuel cell (ADMFC). The results show that changing the cation structures of AEIs has a significant role in MOR on the PtRu/C catalyst. Moreover, with the use of a TPN membrane and the prepared anode containing AEIs, high power densities are achieved with <1 mg_PtRu/cm² in the catalyst layer.

Application of C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Formula: C5H8N2.

Giri, Chandan;Sisk, Sarah E.;Reisman, Louis;Kammakakam, Irshad;Bara, Jason E.;West, Kevin N.;Rabideau, Brooks D.;Rupar, Paul A. research published 《 Anionic Ring-Opening Polymerizations of N-Sulfonylaziridines in Ionic Liquids》, the research content is summarized as follows. The anionic ring-opening polymerization (AROP) of sulfonylaziridines in ionic liquids (ILs) is reported. In imidazolium ILs, the polymerization of 2-methyl-N-tosylaziridine (TsMAz) is not controlled due to poor solubility at higher degree of polymerization and apparent solvent-transfer reactions. In the phosphonium IL [P_6,6,6,14][Tf₂N], the polymerization of TsMAz is controlled and living, and capable of sequential block copolymer synthesis. The polymerization of TsMAz is first-order with respect to monomer in ILs, with rates slower than observed in traditional aprotic polar solvents (e.g., DMF). Mol. dynamics simulations were used to compare DMF vs. IL solutions consisting of BuN(K)Ts (as a model for the propagating chain end). The mol. dynamics simulations suggest better monomer/anion organization in DMF and poorer mobilities in the ILs; both are consistent with observed reduction in polymerization rates in the ILs compared to DMF.

Formula: C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. Their solubility in alcohol is lower than that in water and decreases with increasing molecular weight of the alcohols . Formula: C5H8N2.

Deyko, Grigory S.;Glukhov, Lev M.;Kustov, Leonid M. research published 《 Hydrogen storage in organosilicon ionic liquids》, the research content is summarized as follows. New structures of ionic liquids have been studied as liquid organic hydrogen carriers. The hydrogenation of organosilicon compounds containing a carbazole fragment was carried out for the first time. The N-(CH₂)₃-Si fragment in the composition of the hydrogen carrier based on organosilicon moieties was found to be more suitable than the N-CH₂-Si bond. Ionic liquids with a carbazole fragment containing silicon atoms were synthesized for the first time. It was possible to significantly reduce the m.p. of such ionic liquids by introducing an organosilicon linker between carbazole nitrogen and imidazolium ion. The synthesized ionic liquid is a liquid at room temperature Hydrogenation-dehydrogenation experiments demonstrated that such ionic liquids are thermally stable up to at least 220°C, and nearly quant. conversion can be achieved. Both the hydrogenation and dehydrogenation processes were carried out using the same Pd/C catalyst. The theor. total gravimetric hydrogen capacities for synthesized ionic liquids are 2.05% and 1.58%.

Formula: C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole based anticancer drug find applications in cancer chemotherapy. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Domanski, Michal;Zurauskas, Jonas;Barham, Joshua P. research published 《 Tunable Microwave Flow System for Scalable Synthesis of Alkyl Imidazolium-type Ionic Liquids》, the research content is summarized as follows. A continuous flow auto-frequency tuning single-mode microwave reactor is disclosed as a powerful platform to synthesize alkyl imidazolium salts, e.g., I and II, as ionic liquids/ionic liquid precursors in up to near-quant. yields, 100-600 g h^-1 productivities with record space-time yields. Challenges faced, including viscosity changes, dielec. property changes, and phase separation, were addressed by different operation modes of the reactor without reactor redesigning. Depending on the purpose, this highly productive method could prove to be useful for intensive applications of ionic liquids

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Recommanded Product: 1,2-Dimethyl-1H-imidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. HPLC of Formula: 1739-84-0.

Eftaiha, Ala′a F.;Qaroush, Abdussalam K.;Hasan, Areej K.;Helal, Wissam;Al-Qaisi, Feda′a M. research published 《 CO₂ fixation into cyclic carbonates catalyzed by single-site aprotic organocatalysts》, the research content is summarized as follows. CO₂ fixation is a prominent research theme that attracts the attention of scientists, stakeholders and governmental entities with the aim of ultimately bringing com. products to the market. Herein, a series of mono-, bi-functional and polymeric imidazolium-based catalysts were synthesized and utilized for the production of cyclic carbonates (CCs) using epoxides and 1 bar of CO₂ under mild reaction conditions. In addition, three onium salts, namely, ammonium, phosphonium, and pyridinium, were synthesized and characterized using ¹H/¹³C NMR (NMR) and attenuated total reflectance-Fourier transform IR (ATR-FTIR) spectroscopies, together with thermal gravimetric anal. (TGA), high-resolution mass spectrometry (HRMS) and elemental anal. (EA). All the investigated organocatalysts showed almost quant. CC conversions, which were isolated from the crude reaction and identified spectroscopically. D. functional theory (DFT) calculations revealed that the aforementioned onium salts followed the same detailed mechanism for the cycloaddition reaction, which started with the electrostatic interaction of the onium centers with the oxygen atom of the epoxide. Even in the case of the imidazolium nucleus, the acidic C₂ proton played a marginal role in the epoxide activation than in the ring-opening step.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., HPLC of Formula: 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a five-membered heterocyclic moiety that possesses three carbon, two nitrogen, four hydrogen atoms, and two double bonds. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is also known as 1, 3-diazole. It contains two nitrogen atoms, in which one nitrogen bear a hydrogen atom, and the other is called pyrrole type nitrogen. Computed Properties of 1739-84-0.

El Seoud, Omar A.;Bioni, Thais A.;Dignani, Marcella T. research published 《 Understanding cellulose dissolution in ionic liquid-dimethyl sulfoxide binary mixtures: Quantification of the relative importance of hydrogen bonding and hydrophobic interactions》, the research content is summarized as follows. We studied the dissolution of microcrystalline cellulose (MCC) in mixtures of DMSO with 32 ionic liquids (ILs), at a fixed temperature (70°C) and mole fraction of DMSO (χ_DMSO = 0.6). Under these conditions, employing a recommended dissolution protocol, MCC dissolved in 19 IL-DMSO mixtures In order to access quant. the relative importance (to biopolymer dissolution) of cellulose-solvent interactions, we correlated the mass fraction of dissolved cellulose (MCC-m%) with physicochem. properties of these mixtures The solvent descriptors that gave the best correlations are Lewis acidity and Lewis basicity (calculated from the UV-Vis spectra of solvatochromic probes), the molar volume of the IL, and the Lorentz-Lorenz refractive index function of the IL-DMSO mixtures This result is similar to that observed when solvent empirical polarities of these binary mixtures were correlated with the same descriptors. The multi-parameter correlations quantify, for the first time, the relative importance of cellulose-solvent interactions. Our results agree with the established opinion that an efficient cellulose solvent should disrupt the inter- and intramol. hydrogen bonding in cellulose, and the hydrophobic interactions present due to the amphiphilic nature of the biopolymer.

Computed Properties of 1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. Their solubility in alcohol is lower than that in water and decreases with increasing molecular weight of the alcohols . Formula: C5H8N2.

Deyko, Grigory S.;Glukhov, Lev M.;Kustov, Leonid M. research published 《 Hydrogen storage in organosilicon ionic liquids》, the research content is summarized as follows. New structures of ionic liquids have been studied as liquid organic hydrogen carriers. The hydrogenation of organosilicon compounds containing a carbazole fragment was carried out for the first time. The N-(CH₂)₃-Si fragment in the composition of the hydrogen carrier based on organosilicon moieties was found to be more suitable than the N-CH₂-Si bond. Ionic liquids with a carbazole fragment containing silicon atoms were synthesized for the first time. It was possible to significantly reduce the m.p. of such ionic liquids by introducing an organosilicon linker between carbazole nitrogen and imidazolium ion. The synthesized ionic liquid is a liquid at room temperature Hydrogenation-dehydrogenation experiments demonstrated that such ionic liquids are thermally stable up to at least 220°C, and nearly quant. conversion can be achieved. Both the hydrogenation and dehydrogenation processes were carried out using the same Pd/C catalyst. The theor. total gravimetric hydrogen capacities for synthesized ionic liquids are 2.05% and 1.58%.

Formula: C5H8N2, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., 1739-84-0.

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole based anticancer drug find applications in cancer chemotherapy. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Domanski, Michal;Zurauskas, Jonas;Barham, Joshua P. research published 《 Tunable Microwave Flow System for Scalable Synthesis of Alkyl Imidazolium-type Ionic Liquids》, the research content is summarized as follows. A continuous flow auto-frequency tuning single-mode microwave reactor is disclosed as a powerful platform to synthesize alkyl imidazolium salts, e.g., I and II, as ionic liquids/ionic liquid precursors in up to near-quant. yields, 100-600 g h^-1 productivities with record space-time yields. Challenges faced, including viscosity changes, dielec. property changes, and phase separation, were addressed by different operation modes of the reactor without reactor redesigning. Depending on the purpose, this highly productive method could prove to be useful for intensive applications of ionic liquids

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Recommanded Product: 1,2-Dimethyl-1H-imidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents. HPLC of Formula: 1739-84-0.

Eftaiha, Ala′a F.;Qaroush, Abdussalam K.;Hasan, Areej K.;Helal, Wissam;Al-Qaisi, Feda′a M. research published 《 CO₂ fixation into cyclic carbonates catalyzed by single-site aprotic organocatalysts》, the research content is summarized as follows. CO₂ fixation is a prominent research theme that attracts the attention of scientists, stakeholders and governmental entities with the aim of ultimately bringing com. products to the market. Herein, a series of mono-, bi-functional and polymeric imidazolium-based catalysts were synthesized and utilized for the production of cyclic carbonates (CCs) using epoxides and 1 bar of CO₂ under mild reaction conditions. In addition, three onium salts, namely, ammonium, phosphonium, and pyridinium, were synthesized and characterized using ¹H/¹³C NMR (NMR) and attenuated total reflectance-Fourier transform IR (ATR-FTIR) spectroscopies, together with thermal gravimetric anal. (TGA), high-resolution mass spectrometry (HRMS) and elemental anal. (EA). All the investigated organocatalysts showed almost quant. CC conversions, which were isolated from the crude reaction and identified spectroscopically. D. functional theory (DFT) calculations revealed that the aforementioned onium salts followed the same detailed mechanism for the cycloaddition reaction, which started with the electrostatic interaction of the onium centers with the oxygen atom of the epoxide. Even in the case of the imidazolium nucleus, the acidic C₂ proton played a marginal role in the epoxide activation than in the ring-opening step.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., HPLC of Formula: 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Imidazole based anticancer drug find applications in cancer chemotherapy. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Quality Control of 1739-84-0.

Chen, Pinghua;Li, Songyuan;Tang, Xiaoqiu;Zheng, Huitao;Shi, Jinwen;Wen, Linyuan;Xu, Yong;Fominski, Vyacheslav;Jiang, Hualin research published 《 Photo-inactive ZIF-8 is applied to significantly enhance the photocatalytic water reduction by forming a built-in electric field with g-C₃N₄ and the mechanism analysis》, the research content is summarized as follows. It has been found in this study that the combination of ZIF-8 and g-C₃N₄ turns the photo-inactive ZIF-8 into ”active” and significantly enhances the photocatalytic performance for H₂ production The exptl. results such as contact p.d. (CPD) and photodeposition anal. suggest that a built-in elec. field exists at the interface of g-C₃N₄ and ZIF-8, and the direction is from ZIF-8 to g-C₃N₄. Furthermore, the theor. calculation of charge d. difference and work functions uncover the potential forming mechanism of the built-in elec. field. The mechanism anal. exhibits that the built-in elec. field is conducive to promote the directional transfer of photo-induced electrons from g-C₃N₄ to ZIF-8, which significantly boosts the catalytic ability. Hence, the construction of a built-in elec. field is considered to be an effective strategy to synthesize robust photocatalysts, and the strategy can be extended to prepare a range of advanced catalysts needing directional charge transfer.

1739-84-0, 1,2-Dimethylimidazole is used in the synthesis of 1,2-dimethyl-3-n-butylimidazoliumchloride and 1,2-dimethyl-3-n-propylimidazolium chloride. It also can be used in the synthesis of 1-(2-methoxyethyl)-2,3-dimethylimidazolium chloride and hexafluorophosphate salts.
1,2-Dimethylimidazole is a heterocyclic compound that contains nitrogen and carbon. It can be produced by the reaction between glyoxal and fatty acid in the presence of a base. 1,2-Dimethylimidazole has been shown to have biological properties such as an antioxidant effect. It is also used as a chemical intermediate for production of other chemicals such as 2-methylimidazole and 3-methylimidazole. 1,2-Dimethylimidazole has been shown to react with metal carbonyls to produce methylimines, which are useful intermediates in organic synthesis. The reaction mechanism involves hydrogen bonding and steric interactions between the imidazole ring and the metal carbonyl reactant., Quality Control of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem