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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 Synthetic study on some imidazole analogues and their antimicrobial activity. Author is Nandini, K.; Kumar, N. K. Hemanth; Basavaraju, Y. B..

In the present research work,some imidazole analogs were synthesized. The structures of newly synthesized compounds were confirmed by spectral data and their antimicrobial activity was tested using Streptomycin and Fluconazole as a standard drug.

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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 Sulfonated-polyvinyl amine coated on Fe3O4 nanoparticles: a high-loaded and magnetically separable acid catalyst for multicomponent reactions, the main research direction is sulfonated polyvinyl amine coated iron oxide nanoparticle catalyst property; multicomponent reaction imidazole synthesis.Product Details of 484-47-9.

In this study, a PVAm-bearing SO3H groups/Fe3O4 nanocomposite was prepared via a simple and in situ polymerization of acrylamide onto the surface of magnetic nanoparticles without using organosilane precursors. In order to obtain amine-functionalized magnetic, Hofmann degradation was carried out. In the following, sulfonated-polyvinyl amine coated on Fe3O4 nanoparticles was prepared by covalent grafting of chlorosulfonic acid on amine groups. The introduction of polymer to the surface of magnetic nanoparticles increases the loading content with functional groups extremely. The resulting hybrid material was effectively employed as an unprecedented acid magnetic catalyst for the one-pot synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles under solvent-free conditions. High yields, mild reaction conditions, short reaction times, operational simplicity with reusability are the notable features of the catalyst. The structure of the newly developed catalyst was characterized using TGA, FT-IR, SEM, TEM, VSM, EDX, CHNS, and XRD anal. Magnetic separation and recycling of the catalyst for at least 8 runs is possible without any significant deterioration in catalytic activity. This work is the first report of employing PVAm as a linker for immobilizing liquid acid on a support.

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Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Article, Research Support, Non-U.S. Gov’t, Nature Communications called Thermochemiluminescent peroxide crystals, Author is Schramm, Stefan; Karothu, Durga Prasad; Lui, Nathan M.; Commins, Patrick; Ahmed, Ejaz; Catalano, Luca; Li, Liang; Weston, James; Moriwaki, Taro; Solntsev, Kyril M.; Naumov, Pance, which mentions a compound: 484-47-9, SMILESS is C1(C2=CC=CC=C2)=NC(C3=CC=CC=C3)=C(C4=CC=CC=C4)N1, Molecular C21H16N2, Related Products of 484-47-9.

Chemiluminescence, a process of transduction of energy stored within chem. bonds of ground-state reactants into light via high-energy excited intermediates, is known in solution, but has remained undetected in macroscopic crystalline solids. By detecting thermally induced chemiluminescence from centimeter-size crystals of an organic peroxide here we demonstrate direct transduction of heat into light by thermochemiluminescence of bulk crystals. Heating of crystals of lophine hydroperoxide to ~115 ° results in detectable emission of blue-green light with maximum at 530 nm with low chemiluminescent quantum yield [(2.1 ± 0.1) x 10-7 E mol-1]. Spectral comparison of the thermochemiluminescence in the solid state and in solution revealed that the solid-state thermochemiluminescence of lophine peroxide is due to emission from deprotonated lophine. With selected 1,2-dioxetane, endoperoxide and aroyl peroxide we also establish that the thermochemiluminescence is common for crystalline peroxides, with the color of the emitted light varying from blue to green to red.

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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 Sugar-Catalyzed Synthesis of Triarylimidazoles-An Exemplary Model of Sweet Chemistry, published in 2020-03-31, which mentions a compound: 484-47-9, Name is 2,4,5-Triphenylimidazole, Molecular C21H16N2, SDS of cas: 484-47-9.

A fine, green and efficient method was proposed for the synthesis of 2-aryl-4,5-diphenyl-1H-imidazoles I [Ar = 2-furyl, Ph, 4-ClC6H4, etc.] using various sugars such as glucose, fructose, sucrose, lactose and maltose as catalysts. The synthesis were carried out under very mild conditions in ethanol at room temperature, and the products were isolated in almost quant. yield with a high purity.

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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.Sutar, Suraj M.; Prabhala, Pavankumar; Savanur, Hemantkumar M.; Kalkhambkar, Rajesh G.; Aridoss, Gopalakrishnan; Laali, Kenneth K. researched the compound: 2,4,5-Triphenylimidazole( cas:484-47-9 ).Quality Control of 2,4,5-Triphenylimidazole.They published the article 《Copper-Catalyzed Coupling of Arylethynes and Aryltriazenes to Access Libraries of 1,2-Diketones and Their Efficacy in Synthesis of Triaryloxazoles, Imidazoles and Diaryl-Diazepines》 about this compound( cas:484-47-9 ) in ChemistrySelect. Keywords: diaryl diazepine preparation; diamine diaryl diketone heterocyclization; triaryloxazole preparation; benzylamine diaryl diketone preparation tandem heterocyclization; imidazole preparation; aryl aldehyde diaryl diketone preparation heterocyclization; arylethyne aryltriazene oxidative coupling copper catalyst. We’ll tell you more about this compound (cas:484-47-9).

Libraries of diaryl-1,2-diketones RC6H4C(O)C(O)C6H4R1 (R = H, 3-Me, 4-Cl, 4-Br, etc.; R1 = H, 4-Br, 4-Cl, 4-Me, etc.) were synthesized by oxidative coupling of 1-aryl-ethynes RC6H4CCH with 1-aryl-triazenes R1C6H4N=NR2 (R2 = piperidin-1-yl, morpholin-4-yl, pyrrolidin-1-yl), employing tetramethylguanidinium ionic liquid [TMG][CF3COO] and Cu(OAc)2. The synthesized compounds served as scaffolds for facile one-pot synthesis of diverse libraries of pharmaceutically important heterocycles I (R3 = Ph, 4-chlorophenyl, furan-2-yl, etc.), II (R4 = H, Me, OMe, Cl, Br) and III in ionic liquid solvents. Thus BMIM-ionic liquid/CuI was utilized for the synthesis of triaryl-oxazoles I, [TMG][HSO4]/NH4OAc was used to prepare triaryl-imidazoles II, and [TMG][OAc] was employed for the synthesis of diaryl-diazepines III. Reactions were performed in fresh as well as in recycled ionic liquids The reported methods expand the available protocols for the synthesis of diaryl-1,2-diketones, and enable facile access to pharmaceutically important nitrogen heterocycles I, II and III.

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Application In Synthesis of 2,4,5-Triphenylimidazole. 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 Fe3O4/SO3H@zeolite-Y as a novel multi-functional and magnetic nanocatalyst for clean and soft synthesis of imidazole and perimidine derivatives. Author is Kalhor, Mehdi; Zarnegar, Zohre.

In this study, SO3H@zeolite-Y was synthesized by the reaction of chlorosulfonic acid with zeolite-NaY under solvent-free conditions, which was then supported by Fe3O4 nanoparticles to give SO3H@zeolite-Y (Fe3O4/SO3H@zeolite-Y) magnetic nanoparticles. Several techniques were used to evaluate the phys. and chem. characterizations of the zeolitic nanostructures. Fe3O4-loaded sulfonated zeolite was applied as a novel multi-functional zeolite catalyst for the synthesis of imidazole and perimidine derivatives This efficient methodol. has some advantages such as good to excellent yield, high purity of products, reusability of nanocatalyst, simple reaction conditions, environmental friendliness and an economical chem. procedure from the viewpoint of green chem.

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The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 2,4,5-Triphenylimidazole, is researched, Molecular C21H16N2, CAS is 484-47-9, about New phosphonium molybdate-promoted green, fast and selective catalytic procedure for the synthesis of trisubstituted imidazoles, the main research direction is triaryl imidazole preparation selective green chem; benzil aromatic aldehyde cyclocondensation phosphonium molybdate catalyst; ethane diyl ditriphenylphosphonium hexamolybdate dimethylsulfoxide preparation antibacterial.Quality Control of 2,4,5-Triphenylimidazole.

The compound 1,1′-(ethane-1,2-diyl)ditriphenylphosphonium hexamolybdate dimethylsulfoxide [C2H4[P(C6H5)3]2][Mo6O19].SO(CH3)2 (I) was prepared, and single crystal X-ray diffraction anal. was used to characterize the titled compd (I). Crystallog. data showed that compound (I) crystallized in the monoclinic crystal system in C2/c space group. The compound (I) was used for selective synthesis of 2,4,5-tri aryl imidazole derivatives I (R = Ph, furan-2-yl, 1-naphthyl, etc.) under solvent-free conditions efficiently. Because of hindrance of the catalyst, the yields of products for aldehydes RCHO bearing para substituents are higher than the aldehydes bearing ortho substituents, and for aromatic aldehydes with meta substituents are very low.

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HPLC of Formula: 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 Synthesis of Tri- and Tetra- Phenyl Substituted 1H-imidazoles in the Presence of Chitin and Pectin as Natural Catalyst.

Chitin and pectin are important natural polymers which are used as a natural catalyst for the synthesis of tri- and tetra- Ph substituted 1H-imidazoles I (Ar = Ph, 2-chlorophenyl, naphthalen-1-yl, thiophen-2-yl, etc.; R = H, Ph, Bn, 4-chlorophenyl, 4-bromophenyl). The reaction of benzil and aromatic aldehydes ArCHO with ammonium acetate in the presence of chitin produces 2,4,5-triphenyl-1H-imidazoles I (R = H) and the reaction of benzil, aromatic aldehydes and aniline derivatives RNH2 with ammonium acetate in the presence of pectin produces 1,2,4,5- tetraphenyl-1H-imidazoles I (R = Ph, Bn, 4-chlorophenyl, 4-bromophenyl), resp. All synthesized compounds I are in good agreement with previously reported compounds

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Fekri, Leila Zare; Nateghi-Sabet, Maryam published the article 《1,4-diazabicyclo[2.2.2]octanium diacetate: an effective, mild and reusable catalyst for the synthesis of 2,4,5-trisubstituted imidazoles》. Keywords: trisubstituted imidazole preparation diazabicyclooctanium diacetate catalyst green chem; benzil benzoin ammonium acetate aldehyde multicomponent condensation.They researched the compound: 2,4,5-Triphenylimidazole( cas:484-47-9 ).Recommanded Product: 2,4,5-Triphenylimidazole. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:484-47-9) here.

1,4-Diazabicyclo[2.2.2]octanium diacetate supplies an environmentally friendly procedure for the synthesis of 2,4,5-trisubstituted imidazoles through one-pot multicomponent condensation of benzyl or benzoin and ammonium acetate with various aldehydes. These compounds were obtained in high yields and short reaction times. The catalyst could be easily recovered and reused for five cycles with almost consistent activity.

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In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Novel and reusable mesoporous silica supported 4-methylbenzenesulfonate-functionalized ionic liquids for room temperature highly efficient preparation of 2,4,5-triaryl-1H-imidazoles, published in 2021, which mentions a compound: 484-47-9, mainly applied to mesoporous silica methylbenzenesulfonate ionic liquid catalyst reusable; triarylimidazole green preparation; benzil benzaldehyde condensation titanium mesoporous silica ionic liquid, Application In Synthesis of 2,4,5-Triphenylimidazole.

A series of mesoporous material-supported ionic liquids were prepared and tested as effective and practical catalysts for the synthesis of 2,4,5-triaryl-1H-imidazoles I [R = H, 4-Cl, 2-OH, etc.] using benzil and benzaldehydes. The effects of type of catalysts, catalyst amount, and catalyst stability have also been investigated in detail. The catalyst Ti-SBA-15@ILTsO exhibited excellent activity in excellent yields of 92%9̃9% with low catalyst amount at room temperature within 1 h. In addition, the supported ionic liquid could be easily recovered and reused six times with satisfactory catalytic activity. Furthermore, a general synergetic catalytic mechanism for the reaction was proposed. This work employing Ti-SBA-15@ILTsO as highly efficient and stable catalyst for the synthesis of 2,4,5-triaryl-1H-imidazoles has potential com. applications.

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