Category: 484-47-9

Akamatsu, Masaaki published an article about the compound: 2,4,5-Triphenylimidazole( cas:484-47-9,SMILESS:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1 ).Recommanded Product: 2,4,5-Triphenylimidazole. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:484-47-9) through the article.

A review. Photo-induced morphol. changes in mol. assemblies, formed by surfactants, enable controlled release of incorporated substances, which can be applied in delivery systems of drugs and active components. Here, author review structural anal. of mol. assemblies, formed by azobenzene- or lophine dimer-based surfactants and their function controls with photoirradiation Moreover, author′s current subject regarding rate and dynamics of photoinduced morphol. changes in the mol. assemblies by photoirradiation is discussed.

The article 《Analysis and applications of photo-responsive molecular assemblies》 also mentions many details about this compound(484-47-9)Recommanded Product: 2,4,5-Triphenylimidazole, you can pay attention to it, because details determine success or failure

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Recommanded Product: 2,4,5-Triphenylimidazole. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about Iron-Phosphonate Nanomaterial: As a Novel and Efficient Organic-Inorganic Hybrid Catalyst for Solvent-Free Synthesis of Tri-Substituted Imidazole Derivatives. Author is Arpanahi, Foozhan; Mombeni Goodajdar, Bijan.

In this study, organic-metal nanocatalyst was synthesized by reacting ferric(II) chloride with organic phosphonate ligand. The particle size was controlled with the help of the surfactant. Nanoparticle structure was analyzed using Fourier transform IR, thermogravimetric anal., vibrating sample magnetometer, SEM, dispersive X-ray, Brunauer-Emmett-Teller isotherm and X-ray diffraction spectra. Next, its catalytic activity was investigated in the synthesis of heterocyclic compounds (2,4,5-trisubstituted imidazoles derivatives). Under optimal conditions, the products were obtained with good efficiency and short time. Products identification were evaluated using phys. data, FT-IR, 1H and 13C NMR anal. The results show that the new method, namely the use of iron-phosphonate nanostructures, is effective for the synthesis of trisubstituted imidazole derivatives This method has many advantages such as short reaction time, high yield, solvent free conditions, recyclability of the catalyst, and easy workup.

After consulting a lot of data, we found that this compound(484-47-9)Recommanded Product: 2,4,5-Triphenylimidazole can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Nitrile – Wikipedia,
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Heravi, Majid Momahed; Karimi, Narges; Pooremami, Samira published an article about the compound: 2,4,5-Triphenylimidazole( cas:484-47-9,SMILESS:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1 ).Formula: C21H16N2. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:484-47-9) through the article.

We introduced a very simple, one-pot three component procedure for preparation of 2,4,5-triaryl-imidazoles from the reaction of benzyl, aldehydes and ammonium acetate, as ammonia source, catalyzed by Caro’s acid-silica gel under Solvent -free condition.

After consulting a lot of data, we found that this compound(484-47-9)Formula: C21H16N2 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Application of 484-47-9. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about Magnetic nano cobalt ferrite: an efficient recoverable catalyst for synthesis of 2,4,5-trisubstituted imidazoles. Author is Gupta, Srinivasa; Lakshman, Manisha.

An efficient three-component synthesis of 2,4,5-trisubstituted imidazoles I (X = H, 4-Me, 4-F, etc.) by one pot condensation of aldehydes, diketones and ammonium acetate using CoFe2O4 magnetic nanoparticles as an efficient and environmentally benign catalyst is described. The easy recovery of the catalyst and reusability, broad substrate scopes, high yields of products and ethanol as solvent make this protocol practical, environmentally friendly and economically attractive.

After consulting a lot of data, we found that this compound(484-47-9)Application of 484-47-9 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Name: 2,4,5-Triphenylimidazole. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about Sulfonated Fe3O4@PVA superparamagnetic nanostructure: design, in-situ preparation, characterization and application in the synthesis of imidazoles as a highly efficient organic-inorganic Bronsted acid catalyst. Author is Maleki, Ali; Rahimi, Jamal; Valadi, Kobra.

A new approach for in-situ preparation of Fe3O4@PVA nanostructure as well as its sulfonation was investigated. Then, the functional group of the prepared nanocatalyst was characterized by Fourier transform IR (FT-IR) spectroscopy. The size and morphol. of the nanoparticles were tested by using SEM images. The presence of constructive elements in the nanocomposites was confirmed by energy dispersive X-ray (EDX) anal. To better insight, the structure and magnetic properties of the prepared nanostructure were studied by X-ray diffraction (XRD) pattern and vibrating sample magnetometer (VSM) anal. Thermal stability and weight loss for the nanostructure composition at each step of weight change were screened by thermogravimetric anal. (TGA). Finally, the prepared nanocomposite structure was confirmed by transmission electron microscope (TEM) image. Then, for the first time, Fe3O4@PVA sulfonic acid-based superparamagnetic nanocatalyst was studied for the synthesis of 2,4,5-triarylimidazoles I (R = Ph, 2,4-dichlorophenyl, 2-thienyl, etc.) via a one-pot three-component condensation reaction starting from ammonium acetate, aldehydes RCHO and benzil or benzoin. Due to high magnetic property of the catalyst, it was easily recyclable by a magnet at least for ten runs without any significant reduction in the catalytic activity.

Although many compounds look similar to this compound(484-47-9)Name: 2,4,5-Triphenylimidazole, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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Nitrile – Wikipedia,
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COA of Formula: C21H16N2. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about Ultrasound-assisted synthesis of NiO nanoparticles and their catalytic application for the synthesis of trisubstituted imidazoles under solvent free conditions. Author is Gajengi, Aravind L.; Chaurasia, Shivkumar; Monflier, Eric; Ponchel, Anne; Ternel, Jeremy; Bhanage, Bhalchandra M..

This protocol reported the ultrasound assisted synthesis of NiO nanoparticles(NPs) using benzylamine as a base and different types of cyclodextrins (CDs) as capping agents. The use of α-CD, β-CD or γ-CD leads to different morphologies of NiO NPs. In particular, NiO nanosheets obtained using β-CD as the capping agent. The synthesized NPs were characterized by FEG-SEM, TEM, XRD and EDS anal. They showed high catalytic activity towards synthesis of different trisubstituted imidazoles under solvent free conditions. In addition, NiO NPs could be recycled and reused consecutively up to four recycle runs without much loss of their catalytic activity.

Although many compounds look similar to this compound(484-47-9)COA of Formula: C21H16N2, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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Nitrile – Wikipedia,
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Recommanded Product: 484-47-9. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about CoFe2O4 as green and efficient catalyst for synthesis of multisubstituted imidazoles.

In this study, CoFe2O4 as a highly efficient and eco-friendly catalyst has been developed for three component one-pot synthesis of lophine as the representative of multisubstituted imidazoles. The present methodol. offers several advantages such as excellent yields (99%), short reaction times (10 min) and environmentally mild reaction conditions (500C). Moreover, the catalyst was separated easily by an external magnet and reused several times without significant loss of catalytic properties.

Although many compounds look similar to this compound(484-47-9)Recommanded Product: 484-47-9, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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Nitrile – Wikipedia,
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The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 2,4,5-Triphenylimidazole( cas:484-47-9 ) is researched.Category: nitriles-buliding-blocks.Gabla, Jenifer J.; Lathiya, Dharmesh R.; Revawala, Akash A.; Maheria, Kalpana C. published the article 《Propyl-SO3H functionalized SBA-15: Microwave-mediated green synthesis of biologically active multi-substituted imidazole scaffolds》 about this compound( cas:484-47-9 ) in Research on Chemical Intermediates. Keywords: SBA15 propysulfate catalyst preparation multicomponent heterocyclization catalyst; imidazole multicomponent solventless green synthesis; microwave irradiation multicomponent solventless heterocyclization mediator. Let’s learn more about this compound (cas:484-47-9).

Propylsulfonic acid functionalized Santa Barbara Amorphous-15 (SBA-15-Pr-SO3H) catalyst has been synthesized using a surface modification of mesoporous SBA-15 via the one-pot co-condensation method. The synthesized SBA-15-Pr-SO3H has been characterized by peculiar characterization techniques such as small- and wide-angle XRD, SEM-EDX, TEM, TG-DTA, acidity, FT-IR, Py-FT-IR and BET surface area anal. The catalytic activity of synthesized catalyst has been studied towards solvent-free MW irradiation for the green and rapid synthesis of multi-substituted imidazoles, [2,4,5-triphenyl-1(H)-imidazole (tri-imidazole) and 1-benzyl-2,4,5-triphenyl-1H-imidazole (tetra-imidazole)]. The SBA-15-Pr-SO3H catalyst was found to be an efficient and recyclable solid acid catalyst and this solvent-free MW protocol afforded products in good to excellent yields of both, tri and tetra imidazoles (> 95%) within shorter reaction time (3 min) at 600 W as compared to the SBA-15 and other existing protocols. The applicability of this protocol was further explored by conducting the experiments in the presence of varied solvents and substituted aldehydes to generate a library of both, tri- and tetra-imidazole scaffolds. The catalyst was found to be reusable up to several runs without loss of its catalytic activity. This report allows the rapid and scalable access to a variety of multi-substituted imidazoles using SBA-15-Pr-SO3H, as heterogeneous catalyst.

Although many compounds look similar to this compound(484-47-9)Category: nitriles-buliding-blocks, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Anti-Escherichia Coli Non-Pathogenic Strain Activity Of Complex Compound Based On Copper(II) And 2,4,5-triphenyl-1h-Imidazole, published in 2021, which mentions a compound: 484-47-9, Name is 2,4,5-Triphenylimidazole, Molecular C21H16N2, Computed Properties of C21H16N2.

The complex of Copper(II) binding 2,4,5-triphenyl-1H-imidazole ligand is a new copper complex and exhibits therapeutic properties to bacteria. The present observation is focused on anti-Escherichia coli non-pathogenic strain using disk diffusion method. Copper(II)-2,4,5-triphenyl-1H-imidazole complex compound showed anti-Escherichia coli non-pathogenic strain activity with a range of inhibition zone 14.51-17.37 mm and compared with free metal Cu(II) less reactive with a range of inhibition zone 10.57-27.16 mm, but more no toxic in the Vero cells with CC50 44.74 Μg/mL.

Although many compounds look similar to this compound(484-47-9)Computed Properties of C21H16N2, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 484-47-9, is researched, Molecular C21H16N2, about SO3H-functionalized Zeolite-Y as an Efficient Nanocatalyst for the Synthesis of N-benzimidazole-2-aryl-4-thiazolidinones and tri-substituted Imidazoles, the main research direction is sulfonic acid functionalized zeolite Y nanocatalyst preparation surface structure; aminobenzimidazole benzaldehyde thioglicolic acid zeolite nanocatalyst cyclocondensation green chem; benzoimidazolyl phenyl thiazolidinone preparation; benzil benzaldehyde ammonium acetate sulfonic acid functionalized zeolite cyclocondensation; triphenyl imidazole preparation green chem; 1,3-thiazolidin-4-one; Sulfonated zeolite; aromatic aldehydes; heterogeneous nanocatalyst; imidazole; solid acid..Product Details of 484-47-9.

SO3H-functionalized zeolite-Y was prepared and used as a catalyst for the synthesis of 2-aryl-N-benzimidazole-4-thiazolidinones and tri-substituted imidazoles at ambient conditions. High reaction rates, elimination toxic solvent, simple exptl. procedure and reusability of the catalyst were the important features of this protocol. The SO3H-functionalized zeolite-Y was characterized by FT-IR, FESEM, EDX, XRF and BET. Different kinds of aromatic aldehydes were converted to the corresponding of products with good to excellent yields.

Although many compounds look similar to this compound(484-47-9)Product Details of 484-47-9, numerous studies have shown that this compound(SMILES:C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Nitrile – Wikipedia,
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