Bara, Jason E. et al. published their research in Industrial & Engineering Chemistry Research in 2019 | CAS: 21252-69-7

1-Octyl-1H-imidazole (cas: 21252-69-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Safety of 1-Octyl-1H-imidazole

110th Anniversary: Properties of Imidazolium-Based Ionic Liquids Bearing Both Benzylic and n-Alkyl Substituents was written by Bara, Jason E.;Finotello, Alexia;Magee, Joseph W.;Qian, Shuai;O’Harra, Kathryn E.;Dennis, Grayson P.;Noble, Richard D.. And the article was included in Industrial & Engineering Chemistry Research in 2019.Safety of 1-Octyl-1H-imidazole This article mentions the following:

Reports of imidazolium ionic liquids (ILs) with at least one benzylic substituent bound to the imidazolium cation are far less common than the ubiquitous 1-alkyl-3-methylimidazolium ILs ([Cnmim][X]). Yet, there is significant motivation to determine structure-property relationships for imidazolium-based ILs with at least one benzylic substituent. Not only are these ILs just as straightforward to synthesize as [Cnmim][X] ILs, but ILs with benzylic substituents are also representative segments of poly(ILs) and ionenes where imidazolium cations with benzylic groups are commonly found. This report focuses on the effects of benzyl and methylbenzyl substituents on the d. and viscosity of a series of imidazolium cations paired with bis[(trifluoromethyl)sulfonyl]imide (more commonly known as bistriflimide) ([Tf2N]) anions. Furthermore, the solubility of CO2 in 1-benzyl-3-methylimidazolium bistriflimide [Bnmim][Tf2N] (CAS: 433337-24-7) was measured at 303.15, 318.15, 333.15, and 348.15 K at pressures in the range of 1-9 bar. In the experiment, the researchers used many compounds, for example, 1-Octyl-1H-imidazole (cas: 21252-69-7Safety of 1-Octyl-1H-imidazole).

1-Octyl-1H-imidazole (cas: 21252-69-7) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Safety of 1-Octyl-1H-imidazole

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Alarfaj, N. A. et al. published their research in New Journal of Chemistry in 2018 | CAS: 145040-37-5

1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate (cas: 145040-37-5) belongs to imidazole derivatives. 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. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Application of 145040-37-5

Enhanced SIA-chemiluminescence probes for angiotensin II receptor antagonist detection using silver and gold nanoparticles: applications in pharmaceutical formulations was written by Alarfaj, N. A.;Altamimi, S. A.;El-Tohamy, M. F.;Almahri, A. M.. And the article was included in New Journal of Chemistry in 2018.Application of 145040-37-5 This article mentions the following:

The present work describes three different sequential injection chemiluminescence (SIA-CL) systems (luminol-ferricyanide(III), Ce(IV)-Na2SO3 and luminol-H2O2) for the detection of some angiotensin II receptor antagonists, such as candesartan cilexetil (CDC), valsartan (VAL) and telmisartan (TEL), in their pharmaceutical formulations. Under optimal conditions, CL detection was conducted by measuring the high catalytic potential of silver and gold nanoparticles (AgNPs and AuNPs) in CL oxidation reactions. It was found that the increase in CL signals is proportional to the concentration of the target analytes. The calibration graphs cover linear concentration ranges of 0.001-1000, 0.005-2000 and 0.002-40 ng mL-1 for CDC, VAL and TEL in the presence of AgNPs, resp., and 0.005-500, 0.05-1000 and 0.5-120 ng mL-1, resp. for the previously mentioned drugs in the presence of AuNPs. The influence of possible interfering species such as common cations, amino acids, sugars and coformulated additives was tested. The proposed methods were validated in accordance with the ICH guidelines. The suggested SIA-CL systems were successfully applied to determine the investigated drugs in pure and pharmaceutical dosage forms. The obtained results were in good agreement with those obtained by other reporting methods. In the experiment, the researchers used many compounds, for example, 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate (cas: 145040-37-5Application of 145040-37-5).

1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate (cas: 145040-37-5) belongs to imidazole derivatives. 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. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Application of 145040-37-5

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Lazniewski, Michal et al. published their research in Methods (Amsterdam, Netherlands) in 2022 | CAS: 145040-37-5

1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate (cas: 145040-37-5) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Safety of 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate

Drug repurposing for identification of potential spike inhibitors for SARS-CoV-2 using molecular docking and molecular dynamics simulations was written by Lazniewski, Michal;Dermawan, Doni;Hidayat, Syahrul;Muchtaridi, Muchtaridi;Dawson, Wayne K.;Plewczynski, Dariusz. And the article was included in Methods (Amsterdam, Netherlands) in 2022.Safety of 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate This article mentions the following:

For the last two years, the COVID-19 pandemic has continued to bring consternation on most of the world. According to recent WHO estimates, there have been more than 5.6 million deaths worldwide. The virus continues to evolve all over the world, thus requiring both vigilance and the necessity to find and develop a variety of therapeutic treatments, including the identification of specific antiviral drugs. Multiple studies have confirmed that SARS-CoV-2 utilizes its membrane-bound spike protein to recognize human angiotensin-converting enzyme 2 (ACE2). Thus, preventing spike-ACE2 interactions is a potentially viable strategy for COVID-19 treatment as it would block the virus from binding and entering into a host cell. This work aims to identify potential drugs using an in silico approach. Mol. docking was carried out on both approved drugs and substances previously tested in vivo. This step was followed by a more detailed anal. of selected ligands by mol. dynamics simulations to identify the best mols. that thwart the ability of the virus to interact with the ACE2 receptor. Because the SARS-CoV-2 virus evolves rapidly due to a plethora of immunocompromised hosts, the compounds were tested against five different known lineages. As a result, we could identify substances that work well on individual lineages and those showing broader efficacy. The most promising candidates among the currently used drugs were zafirlukast and simeprevir with an average binding affinity of -22 kcal/mol for spike proteins originating from various lineages. The first compound is a leukotriene receptor antagonist that is used to treat asthma, while the latter is a protease inhibitor used for hepatitis C treatment. From among the in vivo tested substances that concurrently exhibit promising free energy of binding and ADME parameters (indicating a possible oral administration) we selected the compound BDBM50136234. In conclusion, these mols. are worth exploring further by in vitro and in vivo studies against SARS-CoV-2. In the experiment, the researchers used many compounds, for example, 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate (cas: 145040-37-5Safety of 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate).

1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate (cas: 145040-37-5) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Safety of 1-(((Cyclohexyloxy)carbonyl)oxy)ethyl 1-((2′-(2H-tetrazol-5-yl)-[1,1′-biphenyl]-4-yl)methyl)-2-ethoxy-1H-benzo[d]imidazole-7-carboxylate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Chand, Deepak et al. published their research in New Journal of Chemistry in 2019 | CAS: 21252-69-7

1-Octyl-1H-imidazole (cas: 21252-69-7) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Recommanded Product: 21252-69-7

Magnetic ionic liquids based on transition metal complexes with N-alkylimidazole ligands was written by Chand, Deepak;Farooq, Muhammad Qamar;Pathak, Arjun K.;Li, Jingzhe;Smith, Emily A.;Anderson, Jared L.. And the article was included in New Journal of Chemistry in 2019.Recommanded Product: 21252-69-7 This article mentions the following:

In this study, magnetic ionic liquids (MILs) consisting of Ni(II), Co(II), and Mn(II) and paired with the bis[(trifluoromethyl)sulfonyl]imide [NTf2] anion were synthesized from their water soluble chloride intermediates. The MILs feature low viscosity, high hydrophobicity, and hydrolytic stability making them attractive candidates for a number of highly interdisciplinary applications. In the experiment, the researchers used many compounds, for example, 1-Octyl-1H-imidazole (cas: 21252-69-7Recommanded Product: 21252-69-7).

1-Octyl-1H-imidazole (cas: 21252-69-7) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Recommanded Product: 21252-69-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Liu, Yong et al. published their research in Studies in Surface Science and Catalysis in 2007 | CAS: 79917-89-8

1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Product Details of 79917-89-8

One-pot synthesis of ionic liquid functionalized SBA-15 mesoporous silicas was written by Liu, Yong;Peng, Jiajian;Zhai, Shangru;Yu, Ningya;Li, Meijiang;Mao, Jianjiang;Qiu, Huayu;Jiang, Jianxiong;Lai, Guoqiao. And the article was included in Studies in Surface Science and Catalysis in 2007.Product Details of 79917-89-8 This article mentions the following:

1-Methyl-3-n-propyl-imidazolium chloride (MPImCl) and N-propylpyridinium chloride (PPyCl) ionic liquid functionalized SBA-15 mesoporous materials were successfully synthesized through the co-condensation of tetraethoxysilane (TEOS) with 1-methyl-3-(triethoxysilylpropyl)imidazolium chloride (MTESPImCl) and 3-(triethoxysilylpropyl)-pyridinium chloride (TESPPyCl) using EO20PO70EO20 (Pluronic P123) as surfactant. These organic-inorganic hybrid materials may have potential applications in heterogeneous catalysis reactions. In the experiment, the researchers used many compounds, for example, 1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8Product Details of 79917-89-8).

1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Product Details of 79917-89-8

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Venu, kudapa et al. published their research in Tetrahedron in 2022 | CAS: 3012-80-4

1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Safety of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde

New molecular hybrids containing benzimidazole, thiazolidine-2,4-dione and 1,2,4-oxadiazole as EGFR directing cytotoxic agents was written by Venu, kudapa;Saritha, B.;Sailaja, B. B. V.. And the article was included in Tetrahedron in 2022.Safety of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde This article mentions the following:

Herein, some new mol. hybrids having benzimidazole, thiazolidine-2,4-dione and 1,2,4-oxadiazole scaffolds I (Ar = Ph, 3,5-dibromophenyl, 4-pyridyl, etc.) were synthesized from the com. available 1-methyl-1H-benzo[d]imidazole-2-carbaldehyde using two key methodologies such as Knoevenagel condensation and Vilsmeier reagent mediated one-pot synthesis. Further, all the compounds in their μM concentration were screened for their in vitro cytotoxic activity against three human cancer cell lines which includes MCF-7, A-549 and HepG2. Among all, the compound I (Ar = 3,5-dicyanophenyl) exhibited superior activity against all the cell lines as compared to standard drug erlotinib. Besides, the compounds I (Ar = 4-methoxyphenyl, 3,5-dimethoxyphenyl, 4-cyanophenyl) showed superior activity against MCF-7 and most promising activity against A-549 and HepG2 when compared with the pos. control. As well, the tyrosine kinase EGFR inhibitory activity for the potent compounds I (Ar = 4-methoxyphenyl, 3,5-dimethoxyphenyl, 4-cyanophenyl, 3,5-dicyanophenyl), revealed that the compounds I (Ar = 3,5-dimethoxyphenyl, 3,5-dicyanophenyl) displayed nearly double potency as compared to the erlotinib drug. The mol. docking studies of active compounds I (Ar = 4-methoxyphenyl, 3,5-dimethoxyphenyl, 4-cyanophenyl, 3,5-dicyanophenyl) on EGFR target were also conducted and the results were found to be covenant with the corresponding IC50 values. In the experiment, the researchers used many compounds, for example, 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4Safety of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde).

1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde (cas: 3012-80-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Safety of 1-Methyl-1H-benzo[d]imidazole-2-carbaldehyde

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Knierbein, Michael et al. published their research in Organic Process Research & Development in 2020 | CAS: 35487-17-3

1-Methyl-1H-imidazol-3-ium chloride (cas: 35487-17-3) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.COA of Formula: C4H7ClN2

5-Hydroxymethylfurfural Synthesis in Nonaqueous Two-Phase Systems (NTPS)-PC-SAFT Predictions and Validation was written by Knierbein, Michael;Voges, Matthias;Held, Christoph. And the article was included in Organic Process Research & Development in 2020.COA of Formula: C4H7ClN2 This article mentions the following:

The condensation reaction of fructose to 5-hydroxymethylfurfural (HMF) is acid-catalyzed, and it suffers from thermodn. limitation of the conversion, poor kinetics as well as consecutive reactions such as formation of humins from HMF. Different approaches exist to overcome these limitations. In this work, the combination of a non-aqueous solvent and a suitable extraction system is presented that ensures high reaction selectivity at full conversion, fast kinetics, and high partition selectivity of product HMF over reactant fructose, keeping the temperature as low as 70°C. In a first step of the work, the equation of state PC-SAFT was used to predict solvent effects on the reaction equilibrium of homoge-nous reaction systems. It was found that the two hydrophilic ILs [BMIM]Cl and [MIM]Cl shifted the reaction equilibrium to the product side by factors of 230 and 40, resp., compared to the reaction in water. The predictions were verified by exptl. data, which showed full conversion of fructose to HMF within less than 20 (60) minutes for the reaction in [MIM]Cl ([BMIM]Cl) with high selectivity of up to 80%. Even more, the reaction in [MIM]Cl solvent did not require adding catalyst due to the acidic character of this IL. In a second step of this work, an in-situ extraction of HMF was performed using a non-aqueous two-phase reaction system NTPS that was designed with PC-SAFT. The NTPS contains the reaction phase (either [BMIM]Cl or [MIM]Cl) and the extraction agent, i.e. one of the ketones MEK, MIBK, or Et acetate. These IL+organic solvent NTPSs were analyzed and evaluated towards fructose conversion and partitioning of fructose and of HMF. PC-SAFT predicted that among all systems studied in this work, the NTPS IL+MEK was most promising for the reaction of fructose to HMF and the in-situ removal of HMF from fructose. Exptl. results could validate the PC-SAFT predictions; i.e., IL+MEK NTPSs allowed efficient conversion of fructose to HMF and partition selectivity of HMF over fructose of about 100%. This new NTPS does not require addnl. catalyst due to the acidity of [MIM]Cl; it allows high reaction selectivity of 87% at 20 min and 93% conversion, and it moreover provides high separation efficiency. In sum, these results open the door for further developments of in-situ extraction systems in the future for efficient and fast fructose conversion and HMF separation from the reacting phase keeping temperature as low as possible. In the experiment, the researchers used many compounds, for example, 1-Methyl-1H-imidazol-3-ium chloride (cas: 35487-17-3COA of Formula: C4H7ClN2).

1-Methyl-1H-imidazol-3-ium chloride (cas: 35487-17-3) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.COA of Formula: C4H7ClN2

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Landmann, Johannes et al. published their research in Chemistry – A European Journal in 2018 | CAS: 92507-97-6

1-ethyl-2,3-dimethylimidazolium chloride (cas: 92507-97-6) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Name: 1-ethyl-2,3-dimethylimidazolium chloride

Perfluoroalkyltricyanoborate and Perfluoroalkylcyanofluoroborate Anions: Building Blocks for Low-Viscosity Ionic Liquids was written by Landmann, Johannes;Sprenger, Jan A. P.;Hennig, Philipp T.;Bertermann, Ruediger;Gruene, Matthias;Wuerthner, Frank;Ignat’ev, Nikolai V.;Finze, Maik. And the article was included in Chemistry – A European Journal in 2018.Name: 1-ethyl-2,3-dimethylimidazolium chloride This article mentions the following:

The K perfluoroalkyltricyanoborates K[CnF2 n+1B(CN)3] [n =1 (1d), 2 (2d)] and the K mono(perfluoroalkyl)cyanofluoroborates K[CnF2 n+1BF(CN)2] [n =1 (1c), 2 (2c)] and [CnF2 n+1BF2(CN)] [n =1 (1b), 2 (2b), 3 (3b), 4 (4b)] are accessible with perfect selectivities on multi-gram scales starting from K[CnF2 n+1BF3] and Me3SiCN. The K+ salts are starting materials for the preparation of salts with organic cations, for example, [EMIm]+ (EMIm=1-ethyl-3-methylimidazolium). These [EMIm]+ salts are hydrophobic room-temperature ionic liquids (RTILs) that are thermally, chem. and electrochem. very robust, offering electrochem. windows ≤5.8 V. The RTILs described herein, exhibit very low viscosities with a min. of 14.0 mPa s at 20° for [EMIm]1c, low m.ps. down to -57° for [EMIm]2b and extraordinary high conductivities ≤17.6 mS/cm at 20° for [EMIm]1 c. The combination of these properties makes these ILs promising materials for electrochem. devices as exemplified by the application of selected RTILs as component of electrolytes in dye-sensitized solar cells (DSSCs, Graetzel cells). The efficiency of the DSSCs was found to increase with a decreasing viscosity of the neat ionic liquid In addition to the spectroscopic characterization, single crystals of the K salts of the anions 1b-d, 2d, 3b and 4c as well as of [nBu4N]2 c have been studied by x-ray diffraction. In the experiment, the researchers used many compounds, for example, 1-ethyl-2,3-dimethylimidazolium chloride (cas: 92507-97-6Name: 1-ethyl-2,3-dimethylimidazolium chloride).

1-ethyl-2,3-dimethylimidazolium chloride (cas: 92507-97-6) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Name: 1-ethyl-2,3-dimethylimidazolium chloride

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Marszalek, Magdalena et al. published their research in Inorganic Chemistry in 2011 | CAS: 79917-89-8

1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. Imidazole is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Recommanded Product: 1-Methyl-3-propylimidazolium Chloride

Application of Ionic Liquids Containing Tricyanomethanide [C(CN)3] or Tetracyanoborate [B(CN)4] Anions in Dye-Sensitized Solar Cells was written by Marszalek, Magdalena;Fei, Zhaofu;Zhu, Dun-Ru;Scopelliti, Rosario;Dyson, Paul J.;Zakeeruddin, Shaik Mohammed;Gratzel, Michael. And the article was included in Inorganic Chemistry in 2011.Recommanded Product: 1-Methyl-3-propylimidazolium Chloride This article mentions the following:

Novel ionic liquids composed of imidazolium, pyridinium, pyrrolidinium, and NH4+ cations with tricyanomethanide or tetracyanoborate anions were prepared The ionic liquids were characterized by NMR and IR spectroscopy and ESI-mass spectrometry, and their phys. properties were studied. Solid state structures of the N-propyl-N-methylpyrrolidinium and triethylpropylammonium tetracyanoborate salts were obtained by single crystal x-ray diffraction. The salts that are liquid at room temperature were evaluated as electrolyte additives in dye-sensitized solar cells, giving rise to efficiencies 7.35 and 7.85% under 100 and 10% Sun, resp., in combination with the standard Z907 dye. In the experiment, the researchers used many compounds, for example, 1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8Recommanded Product: 1-Methyl-3-propylimidazolium Chloride).

1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. Imidazole is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole is incorporated into many important biological compounds. The most pervasive is the amino acid histidine, which has an imidazole side-chain. Histidine is present in many proteins and enzymes, e.g. by binding metal cofactors, as seen in hemoglobin.Recommanded Product: 1-Methyl-3-propylimidazolium Chloride

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Niedzicki, Leszek et al. published their research in Physical Chemistry Chemical Physics in 2014 | CAS: 79917-89-8

1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Recommanded Product: 79917-89-8

Lithium cation conducting TDI anion-based ionic liquids was written by Niedzicki, Leszek;Karpierz, Ewelina;Zawadzki, Maciej;Dranka, Maciej;Kasprzyk, Marta;Zalewska, Aldona;Marcinek, Marek;Zachara, Janusz;Domanska, Urszula;Wieczorek, Wladyslaw. And the article was included in Physical Chemistry Chemical Physics in 2014.Recommanded Product: 79917-89-8 This article mentions the following:

We present the synthesis route and electrochem. properties of new class of ionic liquids (ILs) obtained from lithium derivate TDI (4,5-dicyano-2-(trifluoromethyl)imidazolium) anion. ILs synthesized by us were EMImTDI, PMImTDI and BMImTDI, i.e. TDI anion with 1-alkyl-3-methylimidazolium cations, where alkyl meant Et, Pr and Bu groups. TDI anion contains fewer fluorine atoms than LiPF6 and thanks to C-F instead of P-F bond, they are less prone to emit fluorine or hydrogen fluoride due to the rise in temperature Use of IL results in non-flammability, which is making such electrolyte even safer for both application and environment. The thermal stability of synthesized compounds was tested by DSC and TGA and no signal of decomposition was observed up to 250 °C. The LiTDI salt was added to ILs to form complete electrolytes. The structures of tailored ILs with lithium salt were confirmed by X-ray diffraction patterns. The electrolytes showed excellent properties regarding their ionic conductivity (over 3 mS cm-1 at room temperature after lithium salt addition), lithium cation transference number (over 0.1), low viscosity and broad electrochem. stability window. The ionic conductivity and viscosity measurements of pure ILs are reported for reference In the experiment, the researchers used many compounds, for example, 1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8Recommanded Product: 79917-89-8).

1-Methyl-3-propylimidazolium Chloride (cas: 79917-89-8) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Recommanded Product: 79917-89-8

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem