Category: 1739-84-0

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 . SDS of cas: 1739-84-0.

Zhao, Shizhen;Yang, Hongkun;Zhao, Bin;Cao, Lifang;Wang, Dong;Russell, Thomas P. research published 《 Homogenizing Blends of Cross-linked Polymers by Interfacial Exchange Reactions》, the research content is summarized as follows. Obtaining homogeneous blends of two covalently crosslinked polymers by mech. mixing is not possible due to their permanent network topologies. Here, we demonstrate an effective route to prepare polymer blends from the common crosslinked epoxidized natural rubber (ENR) and epoxy resin vitrimer (EV) by mech. mixing. Interfacial exchange reactions between these two networks occur by a dynamic transesterification. The as-prepared ENR-EV blends show excellent mech. strength, extensibility, and thermal stability. Moreover, they also show typical vitrimeric properties, including self-healing, welding, and reprocessability. This work demonstrates a large-scale preparation of vitrimeric materials with high performance and versatility from com. available polymers and affords a promising strategy to recycle both waste rubbers and resins.

SDS of cas: 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 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). Application In Synthesis of 1739-84-0.

Zhao, Shizhen;Yang, Hongkun;Dong, Genlai;Wang, Dong;Russell, Thomas P. research published 《 Fully Biobased Elastomer Composites with Mechanically Robust, Reprocessable, and Biocompatible Properties》, the research content is summarized as follows. It is of importance, though difficult, to integrate reinforcement, functionalization and recyclability into elastomeric materials. Here we describe a biomass-derived epoxidized natural rubber (ENR) crosslinked with dynamic covalent bonds and reinforced with functional carboxymethyl chitosan (CMCS). The ENR/CMCS composites show enhanced mech. properties and thermal stability, due to the uniform dispersion of the CMCS fillers and strong interfacial interaction between the ENR matrix and fillers. These crosslinked rubbers can undergo topol. network rearrangements through dynamic exchange reactions, endowing the materials with reprocessability and recyclability. Due to the biol. derived and green features of the both polymeric matrix and filler, the fully biobased ENR/CMCS composites also show excellent biocompatibility, which will expand their application in the field of biomaterials.

Application In Synthesis 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

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Related Products of 1739-84-0.

Zhou, Congyu;Yao, Zhengjun;Wei, Bo;Li, Wenying;Li, Zhejia;Tao, Xuewei;Zhou, Jintang research published 《 Facile synthesis of ZIF-67 derived dodecahedral C/NiCo₂S₄ with broadband microwave absorption performance》, the research content is summarized as follows. The increasing hazard of electromagnetic radiation prompts people to pursue absorbing materials with better performance. However, absorbing materials with a single loss mechanism usually is unable to obtain better absorbing performance due to low impedance matching or high filling ratio. Therefore, this work proposes a C/NiCo₂S₄ (CNCS) material with both dielec. loss/magnetic loss to achieve efficient absorption of electromagnetic waves. The simple preparation of CNCS materials was achieved through the etching of the ZIF-67 template by nickel nitrate and the subsequent hydrothermal vulcanization process. Its unique prismatic dodecahedron hollow structure promotes multiple scattering of electromagnetic waves. The attachment of the magnetic NiCo₂S₄ particles on the surface of the carbon template further promotes the interface polarization and dipole polarization, which is equivalent to the formation of a resistance-rich microcircuit and enhances the effect of the conductance loss on electromagnetic waves. At 2-18 GHz, the CNCS-2 with 30% paraffin addition achieves an effective bandwidth of 5.54 GHz at a matching thickness of 1.7 mm, and has a maximum reflection loss of -36.44 dB at 1.5 mm. By adjusting the thickness of the material matching layer (1-3 mm), an effective bandwidth of up to 13.48 GHz can be achieved, perfectly covering the X-band and Ku-band. Based on the simple preparation process of the material, the special hollow structure and the multiple loss mechanisms for electromagnetic waves, we believe that CNCS can become a strong competitor for high-efficiency broadband absorbers.

Related Products 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 Biochem/physiol Actions: Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division. 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. It also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes. Formula: C5H8N2.

Zhou, Li;Wang, Zhenyu;Xu, Guangqiang;Lv, Chengdong;Wang, Qinggang research published 《 Structure and activity relationship studies of N-heterocyclic olefin and thiourea/urea catalytic systems: application in ring-opening polymerization of lactones》, the research content is summarized as follows. A highly efficient and controllable ring-opening polymerization of lactones (δ-valerolactone, ε-caprolactone and rac-lactide) has been achieved by using N-heterocyclic olefin (NHO) and thiourea/urea (TU/U) catalytic systems. This catalytic system showed high ring-opening activity and stereoselectivity, delivering biodegradable polyesters with high chain-end fidelity, controlled mol. weights and narrow molar mass dispersities. A detailed investigation of the structure-activity relationship was performed by exploring five NHOs and fourteen TUs/Us. For a fixed NHO, when the acidity of TUs/Us decreases, the polymerization mechanism changes from the (thio)urea anion to the neutral cooperative activation mode, and the catalytic activity first increases and decreases, displaying a highly effective interval. For a given TU or U, as the basicity of NHOs increases, the catalytic performance improves correspondingly. Besides, highly isoselective ROP of rac-LA (Pm = 0.93) at -78° has been also achieved, highlighting the versatility of the NHO/TU(U) system. These findings enrich the type of TU/U and base organocatalyst.

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 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. HPLC of Formula: 1739-84-0.

Zozik, Yunus;Sevim, Melike;Lafzi, Ferruh;Kilic, Haydar;Metin, Onder research published 《 Magnetically recoverable nickel-palladium alloy nanocatalysts for direct C-H arylation reactions》, the research content is summarized as follows. Novel magnetically recoverable nanocatalyst comprising nickel-palladium (NiPd) alloy nanoparticles (NPs) supported on reduced graphene oxide (rGO) modified with cobalt ferrite (CoFe₂O₄) NPs was fabricated for the direct C-H arylation of imidazopyridine, imidazole, indolizine and furan with aryl halides. To prepare the presented catalyst, rGO nanosheets were first modified with as-synthesized CoFe₂O₄ NPs and then the obtained CoFe₂O₄-rGO nanocomposites served as a support material for the synthesis of bimetallic NiPd alloy NPs at various compositions The obtained CoFe₂O₄-rGO/NiPd nanocatalysts were characterized by many advanced anal. techniques including TEM, STEM-EDS, XRD, XPS, and ICP-MS. Next, to optimize the reaction conditions, CoFe₂O₄-rGO/NiPd nanocatalysts with different alloy compositions and their monometallic counterparts (CoFe₂O₄-rGO/Ni and CoFe₂O₄-rGO/Pd) were initially tested in the direct C-H arylation of imidazopyridine with bromobenzene. Among all tested nanocatalysts under the optimum reaction conditions, CoFe₂O₄-rGO/Ni₂₀Pd₈₀ showed the best catalytic activity in terms of the isolated product yields. The C-H arylation reactions were studied over a broad substrate scope (35 examples from 36 substrates) and gave the related biaryl products in good to excellent yields. Besides a broad substrate scope, the late-stage C-H arylation of zolimidine, a gastroprotective drug, was realized under the optimized reaction conditions. Moreover, the CoFe₂O₄-rGO/Ni₂₀Pd₈₀ nanocatalysts were recovered from the reaction medium using a simple magnet and reused in the C-H arylation reactions up to five consecutive runs without a significant drop in the product yield. This study shows that magnetically recoverable Pd nanoalloys are promising heterogeneous catalysts to be used in sustainable C-H functionalization reactions.

HPLC of Formula: 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

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Recommanded Product: 1,2-Dimethyl-1H-imidazole.

Zeng, Hui;Tang, Zhenghai;Duan, Yun;Wu, Siwu;Guo, Baochun research published 《 Recyclable crosslinked elastomer based on dynamic dithioacetals》, the research content is summarized as follows. Recent progress in introducing elegant dynamic covalent bonds into covalently crosslinked networks enabled the trade-offs between chem. crosslinking and recycling. Thus far, continuous efforts are made to exploit new dynamic chemistries to address the constrains of intricate preparation procedures and need of catalyst additives in creating dynamic covalent networks. In this work, we report an industrially feasible process to prepare catalyst-free malleable elastomers by engineering dithioacetals as the dynamic motifs into a com. diene rubber. Specifically, a dithioacetal-containing diacid (BTA) is synthesized and used as a novel crosslinker for epoxidized natural rubber (ENR), by which dynamic dithioacetals are introduced into the elastomeric networks. Small mol. model study shows that dithioacetal exchange can be conducted at elevated temperature without catalyst. In the BTA crosslinked ENR, the thermoactivated dithioacetal exchange reactions can alter its network topologies in an associative pathway and confer it with remarkable reprocessability. The mech. properties and relaxation rate of the networks can be readily manipulated by varying the dithioacetal concentration

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

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Related Products of 1739-84-0.

Zhang, Zexian;Luo, Guanyu;Zhou, Shiyuan;Zeng, Wenyan;Mei, Tao;Chen, Zihe;Yu, Xuefeng;Xiao, Xiang;Wang, Xianbao research published 《 Reasonably Introduced ZnIn₂S₄@C to Mediate Polysulfide Redox for Long-Life Lithium-Sulfur Batteries》, the research content is summarized as follows. In consideration of the inferior rate performance and low sulfur utilization of lithium-sulfur batteries (LSBs), an effective strategy via combining polar materials with the conductive carbon sulfur host is widely applied. Herein, metal organic framework-derived in situ-developed ZnIn₂S₄@C is innovatively synthesized to mediate lithium polysulfide (LPS) conversion based on high electron conductivity and strong chem. interactions for advanced LSBs. Polar ZnIn₂S₄ possesses strong chemisorption in keeping with the DFT calculation results and catalytic for LPSs, ensuring a high sulfur utilization. Meanwhile, the hollow non-polar carbon frame possessing hierarchical pores not only provides internal space to contain active species but also accommodates efficient electronic transferring and diffusion of lithium ions in the process of cycling. The above advantages make the electrode possess promising stability and good rate performances, achieving long-term and high-rate cycling. Thus, under a sulfur loading of 1.5 mg cm^-2, after 500 cycles, at 2 and 5 C, the as-prepared ZnIn₂S₄@C@S delivers reversible capacities of 734 mA h g^-1 (75.7% of the initial capacity with a dropping rate of 0.015% per cycle) and 504 mA h g^-1 (68.5% of the primal capacity with a dropping rate of 0.029% per cycle), resp. Even at a high sulfur loading of 5.0 mg cm^-2, at 5 C, 65.6% of the initial capacity can be maintained with a low fading rate of 0.430% per cycle after 500 loops with a high Coulombic efficiency of around 99.8%.

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., Related Products of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . 1739-84-0, formula is C5H8N2, Name is 1,2-Dimethyl-1H-imidazole. In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with an increase of the alkyl chain length of the alcohols. Application of C5H8N2.

Yan, Wenjun;Xu, Huoshu;Ling, Min;Zhou, Shiyu;Qiu, Tong;Deng, Yanjun;Zhao, Zhidong;Zhang, Erpan research published 《 MOF-Derived Porous Hollow Co₃O₄@ZnO Cages for High-Performance MEMS Trimethylamine Sensors》, the research content is summarized as follows. Trimethylamine (TMA) sensors based on metal oxide semiconductors (MOS) have drawn great attention for real-time seafood quality evaluation. However, poor selectivity and baseline drift limit the practical applications of MOS TMA sensors. Engineering core@shell heterojunction structures with accumulation and depletion layers formed at the interface is regarded as an appealing way for enhanced gas sensing performances. Herein, we design porous hollow Co₃O₄@ZnO cages via a facile ZIF-67@ZIF-8-derived approach for TMA sensors. These sensors demonstrate great TMA resistive sensing performance (linear response at moderate TMA concentrations (<33 ppm)), and a high sensitivity of ~41 is observed when exposed to 33 ppm TMA, with a response/recovery time of only 3/2 s. This superior performance benefits from the Co₃O₄@ZnO porous hollow structure with maximum heterojunctions and high surface area. Furthermore, great capacitive TMA sensing with linear sensitivity over the full testing concentration range (0.33-66 ppm) and better baseline stability were investigated. A possible capacitive sensing mechanism of TMA polarization was proposed. For practical usage, a portable sensing prototype based on the Co₃O₄@ZnO sensor was fabricated, and its satisfactory sensing behavior further confirms the potential for real-time TMA detection.

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., Application of C5H8N2

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). SDS of cas: 1739-84-0.

Yao, Shan-Shan;Wang, Hong;Jin, Fan-Long;Park, Soo-Jin research published 《 Synthesis of the ionic liquid 1,2-dimethyl-3-butylimidazole bromide salt and its application in phenolic-formaldehyde-resin-based conductive materials》, the research content is summarized as follows. Herein, the ionic liquid 1,2-dimethyl-3-butylimidazole bromide salt ([DMBIm]Br) was synthesized and its chem. structure was characterized via Fourier transform IR and ¹H NMR spectroscopies. Moreover, to improve the elec. property of the phenolic formaldehyde (PF) resin, PF/[DMBIm]Br systems were prepared via a melt blending and compression-curing process. Furthermore, the effect of [DMBIm]Br content on the thermal stabilities, mech. properties, elec. properties, and morphologies of the systems was investigated. The thermal stability of the systems increased with [DMBIm]Br addition The impact strength of the systems improved with increasing [DMBIm]Br content. Addnl., the volume resistance of the systems significantly decreased from 1.02 x 10⁹ to 1.64 x 10⁷ Ω with increasing [DMBIm]Br content from 0 to 1 wt%.

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., SDS of cas: 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. Application In Synthesis of 1739-84-0.

Yin, Wenyan;Zhang, Milin;Liu, Jingyuan;Alali, Khaled Tawfik;Yu, Jing;Zhu, Jiahui;Liu, Peili;Li, Rumin;Wang, Jun research published 《 MOF-derived electrochemical catalyst Cu-N/C for the enhancement of amperometric oxygen detection》, the research content is summarized as follows. Electrochem. sensors using ionic liquids as electrolytes for oxygen detection are now getting more and more attention. Recently, an ionic liquid combined with an electrochem. active catalyst system has become popular for boosting the sensing performance of oxygen sensors. In this work, the imidazolyl-based ionic liquid 1-butyl-2,3-dimethylimidazole bis((trifluoromethyl)sulfonyl)imide [Bmmim][TFSI] is first prepared by a facile two-step method. Subsequently, a transition metal and N-codoped porous carbon oxygen reduction electrochem. catalyst Cu-N/C is synthesized by calcining the Cu-doped ZIF-8 precursor and then blending it in different ratios with the ionic liquid [Bmmim][TFSI] as composite electrolytes for oxygen detection. The composite electrolyte Cu-N/C/[Bmmim][TFSI] exhibits increased responses in cyclic voltammetry (CV) and chronoamperometry (CA) relative to that of the pure ionic liquid Furthermore, the CV and CA data show that 6% Cu-N/C/[Bmmim][TFSI] has the optimum oxygen sensing response with an enhanced reduction peak current, a sensitivity of 0.1678 μA/[% O₂] and a good linear fitting coefficient of 0.9991. In conclusion, the results confirm the success of using Cu-N/C as an electrochem. catalyst composed of the Cu-N/C/[Bmmim][TFSI] electrolyte for improving the responsivity, stability and sensitivity towards a wide range of oxygen concentrations

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., Application In Synthesis of 1739-84-0

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem