Month: September 2022

Tomas, Renato;Kinart, Zdzislaw;Tot, Aleksandar;Papovic, Snezana;Teodora Borovic, Teona;Vranes, Milan published 《Volumetric properties, conductivity and computation analysis of selected imidazolium chloride ionic liquids in ethylene glycol》 in 2022. The article was appeared in 《Journal of Molecular Liquids》. They have made some progress in their research.Safety of 1-Ethyl-3-methyl-1H-imidazol-3-ium chloride The article mentions the following:

In this paper, the influence of the side chain length of five ionic liquids (ILs): 1-methylimidazolium chloride ([C₀mim][Cl]), 1,3-dimethylimidazolium chloride ([C₁mim][Cl]), 1-ethyl-3-methylimidazolium chloride ([C₂mim][Cl]), 1-butyl-3-methylimidazolium chloride ([C₄mim][Cl]) and 1-hexyl-3-methylimidazolium chloride ([C₆mim][Cl]) on the interactions with ethylene glycol (EG) was studied. Based on the measurement of d. and elec. conductivity of the ionic liquid + EG mixture in the temperature range (278.15-313.15) K, the values of apparent molar volume, standard partial molar volumes, apparent molar volume at infinite dilution, Masson′s interaction coefficient, thermal expansion coefficient, limiting apparent molar expansibilities, Heppler′s coefficient, ion association constants, thermodn. parameters of ion-pair formation as well as diffusion coefficient was calculated Exptl. results were supported by mol. dynamic simulations. With the increase of the side chain length, from C0mim+ to C6mim+ cation, ion-dipole interactions on the solvation process decrease, and the influence of solvophobic solvation increases. Ionic liquids [C₀mim][Cl] and [C₁mim][Cl] show structure-breaker properties, [C₄mim][Cl] and [C6mim][Cl] structure-making properties in EG solutions, while [C₂mim][Cl] is borderline. The values of ion association constants in EG are higher than in water. The ion association process is spontaneous for all ionic liquids and entropy-driven. The experimental procedure involved many compounds, such as 1-Ethyl-3-methyl-1H-imidazol-3-ium chloride (cas: 65039-09-0) .

1-Ethyl-3-methyl-1H-imidazol-3-ium chloride(cas: 65039-09-0) is an imidazolium chloride ionic liquid that can be used as:a starting material for the preparation of 1-ethyl-3-methylimidazolium chloride/tetrafluoroborate (EMI.Cl.BF4) molten salt for electrochemical studies; a solvent as well as catalyst for the depolymerization of oak wood lignin.Safety of 1-Ethyl-3-methyl-1H-imidazol-3-ium chloride

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Name: 2-(1H-Benzo[d]imidazol-2-yl)anilineIn 2020, Jadhavar, Pradeep S.;Patel, Kshitij I.;Dhameliya, Tejas M.;Saha, Nirjhar;Vaja, Maulikkumar D.;Krishna, Vagolu Siva;Sriram, Dharmarajan;Chakraborti, Asit K. published 《Benzimidazoquinazolines as new potent anti-TB chemotypes: Design, synthesis, and biological evaluation》. 《Bioorganic Chemistry》published the findings. The article contains the following contents:

In search for new mol. entities as anti-TB agents, the benzimidazoquinazoline polyheterocyclic scaffolds I (R¹ = H, F, Cl, Br, Me, OMe; R² = H, Cl; R³ = H, Cl; R²R³ = -(CH)₄-; R⁴ = H, Me, Et, n-Pr, n-Bu) have been designed adopting the scaffold hopping strategy. Thirty-two compounds I have been synthesized through an improved tandem decarboxylative nucleophilic addition cyclocondensation reaction of o-phenylenediamines 1,2-(NH₂)₂-4- R²C₆H₂R³ with isatoic anhydrides II followed by further cyclocondensation of the intermediately formed 2-(o-aminoaryl)benzimidazoles III with trialkyl orthoformates R⁴C(OEt)₃. The resultant benzimidazoquinazolines I were evaluated in vitro for anti-TB activity against M. tuberculosis H37Rv (ATCC27294 strain). Fourteen compounds exhibiting MIC values in the range of 0.4-6.25μg/mL were subjected to cell viability test against RAW 264.7 cell lines and found to be non-toxic (<30% inhibition at 50μg/mL). The active compounds were further evaluated against INH resistant Mtb strains. The most active compound I (R¹ = Me; R² = R³ = H; R⁴ = n-Pr) [MIC (H37Rv) of 0.4μg/mL] and the compound I (R¹ = R² = R³ = H; R⁴ = n-Pr) [MIC (H37Rv) of 0.78μg/mL] were also found to be active against INH resistant Mtb strain with MIC values of 12.5 and 0.78μg/mL, resp. And 2-(1H-Benzo[d]imidazol-2-yl)aniline (cas: 5805-39-0) was used in the research process.

2-(1H-Benzo[d]imidazol-2-yl)aniline(cas:5805-39-0 Name: 2-(1H-Benzo[d]imidazol-2-yl)aniline) is a chemical reagent used in the synthesis of small molecule inhibitors targeting ubiquitin-like domains for treatments of diseases caused by the cellular accumulation of damaged proteins.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Today I want to share an article with you. The article is 《Aqueous-processable conducting polymer/ionic liquid solutions for highly conductive organic conductors》,you can find this article in 《Molecular Crystals and Liquid Crystals》. The following contents are mentioned:

Herein, we study how the introduction of secondary dopants, ionic liquids (ILs) into an aqueous-processable conducting polymer (CP), pe:PSS [poly(3,4-ethylenedioxythiophene) doped with poly(4-styrenesulfonate)] affects the PEDOT:PSS dispersion states in the solution, based on dynamic light-scattering anal. We also investigate the elec. characteristics of PEDOT:PSS/IL films that are processed from the composite blends with varied IL concentration As a result, we found that the addition of ILs causes growths of PEDOT:PSS dispersions, and there is a relationship between IL-induced dispersion growths and elec. conductivity enhancement. This work could provide a basis for achieving outstanding elec. performance from aqueous-processable CPs.1-Ethyl-3-methyl-1H-imidazol-3-ium chloride (cas: 65039-09-0) were involved in the experimental procedure.

1-Ethyl-3-methyl-1H-imidazol-3-ium chloride(cas: 65039-09-0) is an imidazolium chloride ionic liquid that can be used as:a solvent as well as catalyst for the depolymerization of oak wood lignin; a solvent in the hydrolysis of hemicellulose (xylan) to xylose using Brønsted acid catalysts.Product Details of 65039-09-0

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Spiess, Alex;Brandt, Philipp;Schmitz, Alexa;Janiak, Christoph published 《Water sorption by ionic liquids: Evidence of a diffusion-controlled sorption process derived from the case study of [BMIm][OAc]》. The research results were published in《Journal of Molecular Liquids》 in 2022.Name: 1-Ethyl-3-methyl-1H-imidazol-3-ium chloride The article conveys some information:

The hydrophilicity of ionic liquids (ILs) could be exploited as desiccants or in sorption-driven heat transformation, yet reports of water sorption isotherms of pure ionic liquids are still scarce. Here, water sorption studies for the six pure hydrophilic ionic liquids with 1-ethyl-3-methylimidazolium [EMIm]⁺ or 1-butyl-3-methylimidazolium [BMIm]⁺ cations and acetate [OAc]^–, formate [HCOO]^– or lactate [Lac]^– anions show a steady and high water uptake with a small hysteresis between absorption and desorption over the relative pressure range of p/p₀ = 0 – 0.9 for the first time. Repeated static volumetric sorption measurements with different amounts or different surface area of the example IL [BMIm][OAc] reveal a slow and strongly diffusion-driven sorption process stemming from the absorption of surface-adsorbed water into the bulk IL. Extrapolation of the water uptake to very small IL amounts with negligible kinetic hindrance gives an equilibrium water uptake capacity of over 2100 mg/g(IL) at p/p₀ = 0.9. Gravimetric control experiments at a relative humidity of 75.5% confirm the time-dependence with the IL surface area at the gas-liquid-interface and the amount of the IL to reach the equilibrium uptake of 1040 mg/g at p/p₀ = 0.75. The experimental procedure involved many compounds, such as 1-Ethyl-3-methyl-1H-imidazol-3-ium chloride (cas: 65039-09-0) .

1-Ethyl-3-methyl-1H-imidazol-3-ium chloride(cas: 65039-09-0) is an imidazolium chloride ionic liquid that can be used as:a starting material for the preparation of 1-ethyl-3-methylimidazolium chloride/tetrafluoroborate (EMI.Cl.BF4) molten salt for electrochemical studies; a solvent as well as catalyst for the depolymerization of oak wood lignin.Name: 1-Ethyl-3-methyl-1H-imidazol-3-ium chloride

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Application of 54147-04-5《Reductive methylation of N¹-substituted 4-ethoxycarbonyl-5-imidazoles》 was published in 1980. The authors were Alenin, V. V.;Domkin, V. D., and the article was included in《Zhurnal Obshchei Khimii》. The author mentioned the following in the article:

Reductive methylation of I (R¹ = Me, R² = H, R³ = Et) by CH₂O and NaBH₄ gave I (R¹ = R² = Me, R³ = Et) which was hydrolyzed by base to give I (R¹ = R² = Me, R³ = H). Analogously obtained was I (R¹ = 2,3-O-isopropylidene-β-D-ribofuranosyl, R² = Me, R³ = Et) which was phosphorylated and deblocked to give I (R¹ = 5-O-phospho-β-D-ribofuranosyl, R² = Me, R³ = H). And Ethyl 5-amino-1-methyl-1H-imidazole-4-carboxylate (cas: 54147-04-5) was used in the research process.

Ethyl 5-amino-1-methyl-1H-imidazole-4-carboxylate (cas: 54147-04-5 Application of 54147-04-5) is a synthetic retinoid that has been shown to be effective in the treatment of psoriasis. It inhibits the activation of histone lysine residues and increases the terminal half life of endogenous synthesis.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Wang, Wan-Wan;Wang, Yuan;Wu, Wei-Na;Zhao, Xiao-Lei;Xu, Zhou-Qing;Xu, Zhi-Hong;Li, Xiao-Xia;Fan, Yun-Chang published 《Pyrrole-quinazoline derivative as an easily accessible turn-off optical chemosensor for Cu²⁺ and resultant Cu²⁺ complex as a turn-on sensor for pyrophosphate in almost neat aqueous solution》 in 2020. The article was appeared in 《Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy》. They have made some progress in their research.Computed Properties of C13H11N3 The article mentions the following:

A simple chemosensor, 6-(1H-pyrrol-2-yl)-5,6-dihydro-benzo[4,5]imidazo[1,2-c]quinazoline (1), was synthesized via simple nucleophilic addition reaction coupled with Schiff base condensation. The probe 1 is aggregation-induced emission-active and could be used as an on-off fluorescence sensor toward Cu²⁺ in H₂O/CH₃CN (99.5%, volume/volume) solution Furthermore, the resultant Cu²⁺ complex selectively responded to pyrophosphate (PPi) among various anions based on fluorescent on-off signal. In addition, the probe could be used for detecting Cu²⁺ and PPi in HeLa cells. And 2-(1H-Benzo[d]imidazol-2-yl)aniline (cas: 5805-39-0) was used in the research process.

2-(1H-Benzo[d]imidazol-2-yl)aniline(cas:5805-39-0 Computed Properties of C13H11N3) is a chemical reagent used in the synthesis of small molecule inhibitors targeting ubiquitin-like domains for treatments of diseases caused by the cellular accumulation of damaged proteins.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Donthiboina, Kavitha;Anchi, Pratibha;Gurram, Sowmyasree;Sai Mani, Geeta;Lakshmi Uppu, Jaya;Godugu, Chandraiah;Shankaraiah, Nagula;Kamal, Ahmed published 《Synthesis and biological evaluation of substituted N-(2-(1H-benzo[d]imidazol-2-yl)phenyl)cinnamides as tubulin polymerization inhibitors》 in 2020. The article was appeared in 《Bioorganic Chemistry》. They have made some progress in their research.COA of Formula: C13H11N3 The article mentions the following:

A new series of N-(2-(1H-benzo[d]imidazol-2-yl)phenyl) cinnamides I [R = H, 4-CH₃, 4-F, etc.; R¹ = H, 4-NO₂, 4-Br, etc.] was prepared and evaluated for their in-vitro cytotoxic activity using various cancer cell lines viz.A549 (human non-small cell lung cancer), MDA-MB-231 (human triple neg. breast cancer), B16-F10 (mouse melanoma), BT-474 (human breast cancer), and 4 T1 (mouse triple neg. breast cancer). In the series of tested compounds, I [R = 4-CH₃ ; R¹ = 4-OC₂H₅] showed potent cytotoxic activity against non-small cell lung cancer cell line with IC₅₀ value of 0.29 ± 0.02μM. The cytotoxicity of most potent compound I [R = 4-CH₃ ; R¹ = 4-OC₂H₅] was also tested on NRK-52E (normal rat kidney epithelial cell line) and showed less cytotoxicity compared to cancer cells. Tubulin polymerization assay indicated that the I [R = 4-CH₃ ; R¹ = 4-OC₂H₅] was able to impede the cell division by inhibiting tubulin polymerization Moreover, mol. docking study also suggested the binding of I [R = 4-CH₃ ; R¹ = 4-OC₂H₅] at the colchicine-binding site of the tubulin protein. Cell cycle anal. revealed that the I [R = 4-CH₃ ; R¹ = 4-OC₂H₅] arrests G2/M phase. In addition, I [R = 4-CH₃ ; R¹ = 4-OC₂H₅] induced apoptosis in A549 cell lines was evaluated by various staining studies like acridine orange, DAPI, anal. of mitochondrial membrane potential, annexin V-FITC, and DCFDA assays. The experimental procedure involved many compounds, such as 2-(1H-Benzo[d]imidazol-2-yl)aniline (cas: 5805-39-0) .

2-(1H-Benzo[d]imidazol-2-yl)aniline(cas:5805-39-0 COA of Formula: C13H11N3) is a chemical reagent used in the synthesis of small molecule inhibitors targeting ubiquitin-like domains for treatments of diseases caused by the cellular accumulation of damaged proteins.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Masri, Asiah Nusaibah;Sulaimon, Aliyu Adebayo published 《Amino acid-based ionic liquids as dual kinetic-thermodynamic methane hydrate inhibitor》 in 2022. The article was appeared in 《Journal of Molecular Liquids》. They have made some progress in their research.Related Products of 65039-09-0 The article mentions the following:

Three amino acid-based ionic liquids (AAILs) are synthesized to evaluate their performance as inhibitors. They are 1-ethyl-3-methyl-imidazolium-glutamate (EMIMGlu), 1-(3-cyanopropyl)-3-methyl-imidazolium-glutamate (CPMIMGlu) and 1-butyl-3-methyl-imidazolium-glutamate (BMIMGlu). The structures are clarified using NMR. Evaluation of their methane hydrate inhibitor performance is performed by micro-differential scanning calorimeter at 5-15 MPa. As a baseline, the hydrate dissociation in water is also evaluated. A standard correlation of methane hydrate dissociation in water is successfully developed with a low average absolute error. Addnl., the AAILs behave as both thermodn. (THI) and kinetic (KHI) hydrate inhibitors. They simultaneously shift the HLVE curve to a lower temperature and decelerate the hydrate formation by reducing the hydrate nucleation rate. EMIMGlu shows the highest THI performance by producing an average temperature shift of 1.14 K, followed by CPMIMGlu (0.91 K) and BMIMGlu (0.87 K). Furthermore, the addition of the nitrile group in CPMIMGlu IL has enhanced the kinetic inhibition process. The kinetic inhibition performance represented by the relative inhibition power (RIP) decreases in the trend of CPMIMGlu (1.31), EMIMGlu (1.30) and BMIMGlu (0.063). The mechanism of the inhibition is further studied by utilizing COSMO-RS software through σ-profile and σ-potential to understand the inhibition process at the mol. level. The exptl. results and computational studies reveal that AAILs behave as THI and KHI through the existence of four oxygen atoms in their anions and cyano group in the CPMIM cation. Thermodn. inhibition properties of AAILs are found to be influenced by the polarity of AAILs while the kinetic inhibition properties of AAILs are found to be influenced by the hydrogen-bonding acceptor value of the AAILs.1-Ethyl-3-methyl-1H-imidazol-3-ium chloride (cas: 65039-09-0) were involved in the experimental procedure.

1-Ethyl-3-methyl-1H-imidazol-3-ium chloride(cas: 65039-09-0) is an imidazolium chloride ionic liquid that can be used as:a solvent as well as catalyst for the depolymerization of oak wood lignin; a solvent in the hydrolysis of hemicellulose (xylan) to xylose using Brønsted acid catalysts.Related Products of 65039-09-0

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Related Products of 65039-09-0《Electrodeposition of a dendrite-free 3D Al anode for improving cycling of an aluminum-graphite battery》 was published in 2022. The authors were Li, Junfeng;Hui, Kwan San;Ji, Shunping;Zha, Chenyang;Yuan, Chengzong;Wu, Shuxing;Bin, Feng;Fan, Xi;Chen, Fuming;Shao, Zongping;Hui, Kwun Nam, and the article was included in《Carbon Energy》. The author mentioned the following in the article:

Aluminum-metal batteries show great potential as next-generation energy storage due to their abundant resources and intrinsic safety. However, the crucial limitations of metallic Al anodes, such as dendrite and corrosion problems in conventional aluminum-metal batteries, remain challenging and elusive. Here, we report a novel electrodeposition strategy to prepare an optimized 3D Al anode on carbon cloth with an uniform deposition morphol., low local c.d., and mitigatory volume change. The sym. cells with the 3D Al anode show superior stable cycling (>450 h) and low-voltage hysteresis (∼170 mV) at 0.5 mA cm^-2. High reversibility (∼99.7%) is achieved for the Al plating/stripping. The graphite | | Al-4/CC full batteries show a long lifespan of 800 cycles with 54 mAh g^-1 capacity at a high c.d. of 1000 mA g^-1, benefiting from the high capacitive-controlled distribution. This study proposes a novel strategy to design 3D Al anodes for metallic-Al-based batteries by eliminating the problems of planar Al anodes and realizing the potential applications of aluminum-graphite batteries.1-Ethyl-3-methyl-1H-imidazol-3-ium chloride (cas: 65039-09-0) were involved in the experimental procedure.

1-Ethyl-3-methyl-1H-imidazol-3-ium chloride(cas: 65039-09-0) is an imidazolium chloride ionic liquid that can be used as:a starting material for the preparation of 1-ethyl-3-methylimidazolium chloride/tetrafluoroborate (EMI.Cl.BF4) molten salt for electrochemical studies; a solvent as well as catalyst for the depolymerization of oak wood lignin.Related Products of 65039-09-0

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Product Details of 65039-09-0《Ion-permselective conducting polymer-based electrokinetic generators with maximized utility of green water》 was published in 2022. The authors were Yun, Tae Gwang;Bae, Jaehyeong;Nam, Hyeon Gyun;Kim, Dongyeon;Yoon, Ki Ro;Han, Seung Min;Kim, Il-Doo, and the article was included in《Nano Energy》. The author mentioned the following in the article:

Hydro-elec. technol. has gathered much attention by the virtue of water as the energy source. However, the low energy d. of this technol. severely limits its practical use. Here, we demonstrate a PEDOT:PSS-based transpiration-driven electrokinetic power generator (p-TEPG) that enables the utilization of a wider variety of real-world water resources for maximizing energy generation efficiencies. In addition to the conventional elec. double layer on the material surface, the p-TEPG builds an addnl. p.d. in the polymer matrix by the selective penetration of cations into the matrix that contains sulfonate functional groups. p-TEPG exhibits 80-250% higher energy d. than carbon-based TEPG at the same resistance. Moreover, seawater produced enhanced volumetric energy/power densities (34.36 mJ cm^-3 and 44.70μW cm^-3) and areal energy/power densities (410μJ cm^-2 and 0.45μW cm^-2), resp., compared to DI water on a single p-TEPG device, which is sufficient to charge elec. energy storage systems and directly operate low-powered electronic.1-Ethyl-3-methyl-1H-imidazol-3-ium chloride (cas: 65039-09-0) were involved in the experimental procedure.

1-Ethyl-3-methyl-1H-imidazol-3-ium chloride(cas: 65039-09-0) is an imidazolium chloride ionic liquid that can be used as:a starting material for the preparation of 1-ethyl-3-methylimidazolium chloride/tetrafluoroborate (EMI.Cl.BF4) molten salt for electrochemical studies; a solvent as well as catalyst for the depolymerization of oak wood lignin.Product Details of 65039-09-0

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem