Gu, Chang et al. published their research in CCS Chemistry in 2022 | CAS: 915358-85-9

1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) 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.Computed Properties of C9H15F6N2P

A strategy of stabilization via active energy-exchange for bistable electrochromic displays was written by Gu, Chang;Wang, Xiaojun;Jia, Ai-Bo;Zheng, Hongzhi;Zhang, Weiran;Wang, Yuyang;Li, Minjie;Zhang, Yu-Mo;Zhang, Sean Xiao-An. And the article was included in CCS Chemistry in 2022.Computed Properties of C9H15F6N2P This article mentions the following:

As future energy-saving optoelectronics, bistable electrochromic (EC) materials/devices have high energy efficiency for potential applications as smart windows, displays, and information/energy storage, due to their ability to maintain optical states without consuming energy. However, further development is hindered by the lack of in-depth understanding of related key factors and universally applicable design strategies to achieve bistability. Herein, we report a new strategy based on active energyexchange with the aid of proton-coupled electron transfer, which can dynamically adjust the HOMO /LUMO energy levels of materials to obtain good bistability from traditional nonbistable materials. This strategy was thoroughly studied and proven by taking quinone derivatives and bromocresol green derivatives as examples. The device obtained after further polymerization and optimization showed remarkable bistability, coloration efficiency, and application potential for energy-saving flexible displays. The success, challenges, and cognitive gains of this strategy not only accelerate the development of various energysaving optoelectronic materials/devices, but are also likely to stimulate progress in physics, chem., and materials. In the experiment, the researchers used many compounds, for example, 1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9Computed Properties of C9H15F6N2P).

1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) 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.Computed Properties of C9H15F6N2P

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Makovei, G. L. et al. published their research in Zashchita Metallov in 1983 | CAS: 13060-24-7

2-Octylbenzimidazole (cas: 13060-24-7) 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 derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Recommanded Product: 13060-24-7

Effect of 2-alkylbenzimidazoles on the corrosion-electrochemical behavior of iron in hydrochloric acid was written by Makovei, G. L.;Koroleva, V. R.;Kurmakova, I. N.. And the article was included in Zashchita Metallov in 1983.Recommanded Product: 13060-24-7 This article mentions the following:

The effect was studied of benzimidazole (I) [51-17-2] and its 2-alkyl substituted derivatives on the corrosion-electrochem. behavior of Armco Fe in 2N HCl. A test was also made of the correlation between the π-electron d. of these compounds and the following corrosion-electrochem. parameters: corrosion rate, effective activation energy of the corrosion process on an Armco Fe electrode, the slope of the polarization curves, polarization resistance, steady-state potential and screening effect. The distribution of the π-electron d. for I was calculated by the MO LCAO method and is presented in diagrams. In the experiment, the researchers used many compounds, for example, 2-Octylbenzimidazole (cas: 13060-24-7Recommanded Product: 13060-24-7).

2-Octylbenzimidazole (cas: 13060-24-7) 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 derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Recommanded Product: 13060-24-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Qin, Xinying et al. published their research in Journal of Polymer Materials in 2018 | CAS: 915358-85-9

1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) 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.COA of Formula: C9H15F6N2P

Facile grafting of ionic liquids onto halloysite nanotubes via an atom transfer radical polymerization method was written by Qin, Xinying;Guo, Ziyang;Wang, Chao;Song, Meining;Zhang, Hailei;Wu, Yonggang. And the article was included in Journal of Polymer Materials in 2018.COA of Formula: C9H15F6N2P This article mentions the following:

Ionic liquids (ILs)-based organic-inorganic nanocomposite materials are a new class of hybrid materials which can be used in lithium batteries, fuel cells, dye-sensitized solar cells and pressure sensors. Halloysite nanotubes (HNTs, Al2Si2O5(OH)4·nH2O) are hollow like aluminosilicate clay, similar to commonly used platy clay kaolin, which open up various attractive applications including catalysis, anticorrosion, adsorbent, drug delivery, enzyme immobilization, fiver spinning and so on. However, the inorganic characteristics of clay-based halloysite nanotube result in a limited application in electronic field, making it difficult to capture attentions as extensively as carbon nanotubes. Herein, we develop a feasible and versatiel approach to prepared ILs grafted HNTs, by coupling the arylboronic acid and Al-OH groups on the HNTs. ILs are grafted to the modified HNTs via a typical atom transfer radical polymerization (ATRP) method. The modified halloysite nanotubes (HNTs) are characterized by (FTIR), thermogravimetric anal., SEM and transmission electron microscope. In the experiment, the researchers used many compounds, for example, 1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9COA of Formula: C9H15F6N2P).

1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) 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.COA of Formula: C9H15F6N2P

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Zhang, Jun-Zhen et al. published their research in Yingyong Huaxue in 2007 | CAS: 13060-24-7

2-Octylbenzimidazole (cas: 13060-24-7) 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Product Details of 13060-24-7

Synthesis, characterization and crystal structure of 1-ferrocenesulfonyl-2-long carbon chain alkyl benzimidazole was written by Zhang, Jun-Zhen;Yang, Bin-Qin;Yang, Ya-Ting;Zhang, Bing-Lin. And the article was included in Yingyong Huaxue in 2007.Product Details of 13060-24-7 This article mentions the following:

Six new 1-ferrocenesulfonyl-2-benzimidazole derivatives were prepared from the reaction of ferrocenesulfonyl chloride with benzimidazole derivatives in the presence of dichloromethane and tetrabutylammonium chloride. The reactions of 2-alkylbenzimidazoles [alkyl = Me(CH2)n, n = 5, 6, 7, 8, 10, 14] with ferrocenesulfonyl chloride give 1-ferrocenesulfonyl-2-alkylbenzimidazoles in good yields. The yields of six new ferrocenesulfonyl benzimidazole derivatives were 78-87%. The structures were confirmed by IR, 1H NMR, elemental anal. and MS. The crystal structure was determined via x-ray single crystal diffraction. The compound 1-ferrocenesulfonyl-2-hexylbenzimidazole is the monoclinic system with space group C2/c, and the unit cell parameters are a = 2.825 2(2) nm, b = 0.976 96(7) nm, c = 1.648 28(12) nm, α = 90°, P = 92.053(2)°, γ = 90°, V = 4.546 6(6) nm3, Z = 8, F(000) = 2 024, Mr = 481.40, Dc = 1.407 g/cm3, μ = 0.784 mm-1, R1 = 0.049 5, wR2 = 0.151 7. In the experiment, the researchers used many compounds, for example, 2-Octylbenzimidazole (cas: 13060-24-7Product Details of 13060-24-7).

2-Octylbenzimidazole (cas: 13060-24-7) 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Product Details of 13060-24-7

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Wang, Qiang et al. published their research in European Polymer Journal in 2020 | CAS: 915358-85-9

1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) 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. 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: 915358-85-9

Evaluation of the surface properties of poly(ionic liquid) materials by inverse gas chromatography was written by Wang, Qiang. And the article was included in European Polymer Journal in 2020.Recommanded Product: 915358-85-9 This article mentions the following:

Inverse gas chromatog. (IGC) was used as a tool to evaluate the surface parameters of three poly(1-alkyl-3-vinylimidazolium hexafluorophosphate) (P[CnVIM][PF6], n = 2, 4, 6) materials that were obtained by a free-radical polymerization IGC characterization was carried out at temperatures ranging between 303.15 and 343.15 K for determining the dispersive free energy (γds) as well as the Lewis acidity and basicity parameters of the three materials. The retention behavior of the probes on the surfaces of the three materials was analyzed by plotting the net retention volumes (Vn) of the probes as a function of temperature The dispersive free energy results revealed that all three materials have high γds values and that the γds value decreases in an almost linear fashion with increasing temperature The acid-base data for the three materials confirmed that the surfaces of all three materials can be considered to be amphoteric with a predominantly basic character and that the basicity decreases with increasing alkyl side chain length on the imidazolium backbone. In the experiment, the researchers used many compounds, for example, 1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9Recommanded Product: 915358-85-9).

1-Butyl-3-vinyl-1H-imidazol-3-ium hexafluorophosphate(V) (cas: 915358-85-9) 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. 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: 915358-85-9

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Plewe, Michael B. et al. published their research in Bioorganic & Medicinal Chemistry Letters in 2021 | CAS: 217435-65-9

6-Bromo-8-methylimidazo[1,2-a]pyridine (cas: 217435-65-9) 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. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Recommanded Product: 6-Bromo-8-methylimidazo[1,2-a]pyridine

Discovery of a novel highly potent broad-spectrum heterocyclic chemical series of arenavirus cell entry inhibitors was written by Plewe, Michael B.;Gantla, Vidyasagar Reddy;Sokolova, Nadezda V.;Shin, Young-Jun;Naik, Shibani;Brown, Eric R.;Fetsko, Alexandra;Zhang, Lihong;Kalveram, Birte;Freiberg, Alexander N.;Henkel, Greg;McCormack, Ken. And the article was included in Bioorganic & Medicinal Chemistry Letters in 2021.Recommanded Product: 6-Bromo-8-methylimidazo[1,2-a]pyridine This article mentions the following:

We identified and explored the structure-activity relationship (SAR) of a novel heterocyclic chem. series of arenavirus cell entry inhibitors. Optimized lead compounds, including diphenyl-substituted imidazo[1,2-a]pyridines, benzimidazoles, and benzotriazoles exhibited low to sub-nanomolar potency against both pseudotyped and infectious Old and New World arenaviruses, attractive metabolic stability in human and most nonhuman liver microsomes as well as a lack of hERG K + channel or CYP enzyme inhibition. Moreover, the straightforward synthesis of several lead compounds (e.g., the simple high yield 3-step synthesis of imidazo[1,2-a]pyridine I) could provide a cost-effective broad-spectrum arenavirus therapeutic that may help to minimize the cost-prohibitive burdens associated with treatments for emerging viruses in economically challenged geog. settings. In the experiment, the researchers used many compounds, for example, 6-Bromo-8-methylimidazo[1,2-a]pyridine (cas: 217435-65-9Recommanded Product: 6-Bromo-8-methylimidazo[1,2-a]pyridine).

6-Bromo-8-methylimidazo[1,2-a]pyridine (cas: 217435-65-9) 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. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Recommanded Product: 6-Bromo-8-methylimidazo[1,2-a]pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Jadhvar, Suresh C. et al. published their research in American Journal of PharmTech Research in 2015 | CAS: 478935-29-4

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Application of 478935-29-4

Synthesis and evaluation of anticancer activity of some new 3-aminoalkylated indole derivatives was written by Jadhvar, Suresh C.;Kasraliker, Hanmant M.;Bhusare, Sudhakar R.. And the article was included in American Journal of PharmTech Research in 2015.Application of 478935-29-4 The following contents are mentioned in the article:

An effective and economical protocol was developed for the synthesis of 3-substituted indoles by one-pot three-component coupling reaction of a substituted salicylaldehyde, N-methylaniline and indole using [Hmim] HSO4 as a catalyst. All the synthesized derivatives were evaluated for inhibition of cancer cell. The initial assays indicated that some of the newly synthesized compounds displayed significantly good inhibition activities against human breast cancer cell (MCF7), cell lines compared with the control (Adriamysin), which might be developed as novel lead scaffold for potential anticancer agents. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Application of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Application of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Yu, Dan et al. published their research in Gongye Cuihua in 2009 | CAS: 478935-29-4

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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 Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Reference of 478935-29-4

Synthesis of diethyl maleate catalyzed by acid functionalized ionic liquids was written by Yu, Dan;Guo, Hongyun. And the article was included in Gongye Cuihua in 2009.Reference of 478935-29-4 The following contents are mentioned in the article:

Di-Et maleate was obtained by a reaction of maleic anhydride and anhydrous ethanol in the presence of an ionic liquid [i.e., TEAPS sulfate, N,N,N-triethyl-3-sulfo-1-propanaminium sulfate (1:1)]. Factors influencing the product formation were confirmed and the above-mentioned Di-Et maleate [i.e., (2Z)-2-butenedioic acid 1,4-di-Et ester, 99% yield] was obtained under the following reaction conditions : n(maleic anhydride) : n(ethanol) = 1:4, dosage of ionic liquid = 20% (wt) of maleic anhydride, cyclohexane as water carrier, 115°, reflux and water segregation for 4 h. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Reference of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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 Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Reference of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Tay, Nicholas E. S. et al. published their research in Journal of the American Chemical Society in 2017 | CAS: 870837-70-0

4-(1H-Imidazol-1-yl)-3-methoxybenzaldehyde (cas: 870837-70-0) 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Category: imidazoles-derivatives

Cation Radical Accelerated Nucleophilic Aromatic Substitution via Organic Photoredox Catalysis was written by Tay, Nicholas E. S.;Nicewicz, David A.. And the article was included in Journal of the American Chemical Society in 2017.Category: imidazoles-derivatives The following contents are mentioned in the article:

Nucleophilic aromatic substitution (SNAr) is a direct method for arene functionalization; however, it can be hampered by low reactivity of arene substrates and their availability. Herein we describe a cation radical-accelerated nucleophilic aromatic substitution using methoxy- and benzyloxy-groups as nucleofuges. In particular, lignin-derived aromatics containing guaiacol and veratrole motifs were competent substrates for functionalization. We also demonstrate an example of site-selective substitutive oxygenation with trifluoroethanol to afford the desired trifluoromethylaryl ether. This study involved multiple reactions and reactants, such as 4-(1H-Imidazol-1-yl)-3-methoxybenzaldehyde (cas: 870837-70-0Category: imidazoles-derivatives).

4-(1H-Imidazol-1-yl)-3-methoxybenzaldehyde (cas: 870837-70-0) 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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Category: imidazoles-derivatives

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Gong, D. et al. published their research in Asian Journal of Chemistry in 2010 | CAS: 478935-29-4

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Related Products of 478935-29-4

Regioselectivity for nitrochlorobenzene preparation over imidazolium ionic liquids media using nitric acid was written by Gong, D.;Peng, X.;Sun, Z.. And the article was included in Asian Journal of Chemistry in 2010.Related Products of 478935-29-4 The following contents are mentioned in the article:

Nitrochlorobenzene was regioselectively prepared over imidazolium ionic liquids media by using HNO3 as nitrating agent. A variety of ionic liquids, [Hmim]HSO4, [Hmim]NO3 and [Hmim]CF3CO2 (Hmim = 1-methylimidazolium) were prepared for the improvement of regioselectivity in preparation of mononitrochlobenzene isomers. A high amount of para isomer was achieved when employing [Hmim]HSO4. Ionic liquids were conveniently reused for five times by filtration with excellent yield of mono-nitration products and para-selectivity. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Related Products of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) 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. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Related Products of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem