Tag: M.W:100-200

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels. 10500-57-9, Name is 5,6,7,8-Tetrahydroquinoline, molecular formula is C9H11N. In an article, author is Hagras, Mohamed,once mentioned of 10500-57-9, Application In Synthesis of 5,6,7,8-Tetrahydroquinoline.

Discovery of new quinolines as potent colchicine binding site inhibitors: design, synthesis, docking studies, and anti-proliferative evaluation

Discovering of new anticancer agents with potential activity against tubulin polymerisation is still a promising approach. Colchicine binding site inhibitors are the most relevant anti-tubulin polymerisation agents. Thus, new quinoline derivatives have been designed and synthesised to possess the same essential pharmacophoric features of colchicine binding site inhibitors. The synthesised compounds were tested in vitro against a panel of three human cancer cell lines (HepG-2, HCT-116, and MCF-7) using colchicine as a positive control. Comparing to colchicine (IC50 = 7.40, 9.32, and 10.41 mu M against HepG-2, HCT-116, and MCF-7, respectively), compounds 20, 21, 22, 23, 24, 25, 26, and 28 exhibited superior cytotoxic activities with IC50 values ranging from 1.78 to 9.19 mu M. In order to sightsee the proposed mechanism of anti-proliferative activity, the most active members were further evaluated in vitro for their inhibitory activities against tubulin polymerisation. Compounds 21 and 32 exhibited the highest tubulin polymerisation inhibitory effect with IC50 values of 9.11 and 10.5 nM, respectively. Such members showed activities higher than that of colchicine (IC50 = 10.6 nM) and CA-4 (IC50 = 13.2 nM). The impact of the most promising compound 25 on cell cycle distribution was assessed. The results revealed that compound 25 can arrest the cell cycle at G2/M phase. Annexin V and PI double staining assay was carried out to explore the apoptotic effect of the synthesised compounds. Compound 25 induced apoptotic effect on HepG-2 thirteen times more than the control cells. To examine the binding pattern of the target compounds against the tubulin heterodimers active site, molecular docking studies were carried out.

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Reference:
Quinoline – Wikipedia,
,Quinoline | C9H7N – PubChem

Let¡¯s face it, organic chemistry can seem difficult to learn, Category: quinolines-derivatives, Especially from a beginner¡¯s point of view. Like 90-52-8, Name is 8-Amino-6-methoxyquinoline, molecular formula is quinoxaline, belongs to quinoxaline compound. In a document, author is Liu, Yan, introducing its new discovery.

4CzIPN-Bu-t-Catalyzed Proton-Coupled Electron Transfer for Photosynthesis of Phosphorylated N-Heteroaromatics

4,5,6-Tetrakis (3,6-di-tert- butyl-9H-carbazol-9-yl)-isophthalonitrile (4CzIPN-Bu-t) was developed as a photocatalyst for the phosphorus-radical-initiated cascade cyclization reaction of isocyanides. By using 4CzIPN-Bu-t as catalyst, we developed a visiblelight-induced proton-coupled electron transfer strategy for the generation of phosphorus-centered radicals, via which a wide range of phosphorylated phenanthridines, quinolines, and benzothiazoles were successfully constructed.

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Reference:
Quinoline – Wikipedia,
,Quinoline | C9H7N – PubChem

In an article, author is Gao, Shurong, once mentioned the application of 90-52-8, Name is 8-Amino-6-methoxyquinoline, molecular formula is C10H10N2O, molecular weight is 174.1992, MDL number is MFCD00672902, category is quinoxaline. Now introduce a scientific discovery about this category, COA of Formula: C10H10N2O.

How to select ionic liquids as extracting agents systematically: a special case study for extractive denitrification processes

Extractive denitrification (EDN) of shale oil using ionic liquids (ILs) as the extracting agent has good industrial prospects. In such processes, ILs with higher selectivity to N-compounds and lower solubility in shale oil are desired to improve the EDN efficiency, and reduce the loss of ILs and the contamination of shale oil. In the present study, we employed COSMO-RS to calculate the selectivity of 70 ILs to the typical N-compounds (pyridine, quinoline and indole). The influence of the IL structural characteristics, composition of shale oil and properties of N-compounds are investigated from a micro-level view with the sigma-surface and sigma-profile. The selectivity strongly depends on anionic species and it is greatly influenced by hydrogen bonding (HB) and pi-pi interaction between N-compounds and ILs. ILs composed of [H2PO4](-) and [MeSO3](-) with larger HB donor energy show higher selectivity to the basic N-compounds, while ILs composed of [Ac](-) with larger pi-electron cloud density show higher selectivity to the non-basic N-compounds. Anions with stronger polarity have lower solubility in shale oil. Moreover, experimental determinations of EDN indicated that [C(4)py][H2PO4]/[C(4)mim][H2PO4] and [C(2)mim][Ac]/[C(2)py][Ac] have good EDN performance for quinoline/pyridine with efficiency of 100% and for indole with efficiency of 91%, respectively. This work presents a theoretical basis to design and select ILs having higher selectivity for N-compounds and lower solubility in shale oil for use in denitrification.

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Reference:
Quinoline – Wikipedia,
,Quinoline | C9H7N – PubChem

One of the major reasons for studying chemical kinetics is to use measurements of the macroscopic properties of a system, Safety of 2,3-Dichloroquinoxaline, such as the rate of change in the concentration of reactants or products with time.In a article, mentioned the application of 2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2

Synthesis and antimicrobial activity of some new substituted quinoxalines

A number of new symmetrically and asymmetrically 2,3-disubstituted quinoxalines were synthesized through functionalization of 2,3-dichloroquinoxaline (2,3-DCQ) with a variety of sulfur and/or nitrogen nucleophiles. The structures of the obtained compounds were established based on their spectral data and elemental analysis. The antimicrobial activity for the prepared compounds was investigated against four bacterial species and two fungal strains. The symmetrically disubstituted quinoxalines 2, 3, 4, and 5 displayed the most significant antibacterial activity, while compounds 6a, 6b, and the pentacyclic compound 10 showed considerable antifungal activity. Furthermore, compounds 3f, 6b showed broad antimicrobial spectrum against most of the tested strains.

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Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1316 | ChemSpider

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. HPLC of Formula: C9H8N2. Introducing a new discovery about 6344-72-5, Name is 6-Methylquinoxaline

The Thermolysis of Polyazapentadienes. Part 2. Formation of Quinoxalines from 5-Aryl-1-phenyl-1,2,5-triazapentadienes

Thermolysis in the gas phase of 5-(p-substituted phenyl)-1-phenyl-1,2,5-triazapentadienes at 600 deg C and 10-2 Torr gives 6-substituted quinoxalines.The yield is ca. 30 percent, and is independent of the electronic nature of the substituent.The corresponding 5-(o-substituted) derivatives give 5-substituted quinoxalines, though the yield is lower, and quinoxaline itself is a major contaminant, due to ipso attack and ejection of the substituent. 5-(m-Substituted) derivatives give mixtures of 5- and 6-substituted quinoxalines on pyrolysis.The 5-isomer is dominant for compounds with m-alkyl substituents, while the 6-isomer is the major product for those with electron-withdrawing or electron-donating m-substituents.

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Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N32 | ChemSpider

Application of 59564-59-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 59564-59-9, Name is 3,4-Dihydroquinoxalin-2(1H)-one, molecular formula is C8H8N2O. In a Article£¬once mentioned of 59564-59-9

Reaction of 4-substituted 1,2-phenylenediamine with chloroacetic acid and alpha, beta-unsaturated carboxylic acids: Determination of the structure of the isomers formed using long-range carbon-proton coupling

The reaction between 4-chloro-1,2-phenylenediamine with sodium salt of chloroacetic acid yields 8-chlorotetrahydroquinoxalin-2-one, o-Phenylenediamines substituted at position-4 yield a single benzodiazepinone on reaction with alpha,beta-unsaturated aliphatic carboxylic acids.The structures of the products formed are established from 13C NMR of the products and their acyl derivatives, sometimes, using long range carbon-proton couplings.

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Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N168 | ChemSpider

Reference of 2213-63-0, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a Article£¬once mentioned of 2213-63-0

One-pot Synthesis of Quinoxaline Chalcones from Commercially Available Calcium Carbide Through Palladium-Catalyzed Coupling Reactions

New (E)-3-(2-aminoquinoxalin-3-yl)-1-arylprop-2-en-1-ones are prepared through the multi-component reaction of 3-substituted-2-chloroqunoxalines, calcium carbide, and aromatic aldehydes in the presence of diethylamine, catalyzed by Pd/Cu in acetonitrile. This synthetic strategy presents an acetylene molecule linking the quinoxaline scaffold to an aldehyde moiety for construction of quinoxaline chalcone by two carbon-carbon bond coupling reactions. This one-pot process provides an efficient and direct method for the synthesis of new quinoxaline chalcones from the low-cost calcium carbide with good yields. A number of synthesized compounds were screened for their in vitro anti-bacterial activity against Gram-positive and Gram-negative bacteria using a well-diffusion method.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1556 | ChemSpider

In heterogeneous catalysis, the catalyst is in a different phase from the reactants. Recommanded Product: 15804-19-0, At least one of the reactants interacts with the solid surface in a physical process called adsorption in such a way. 15804-19-0, name is Quinoxaline-2,3(1H,4H)-dione. In an article£¬Which mentioned a new discovery about 15804-19-0

Benzopyrones. Part 23. Cyclization of o-Amino Carboxamides and Related Compounds

Cyclization of 2-amino-6-bromo-4-oxochromene-3-carboxamide (5) with diethyl oxalate-sodium ethoxide gave the benzopyrano<2,3-d>pyrimidine-4,6-dione (6).Ethyl 3-amino-2-carbamoyl-4-oxochromene-6-carboxylate (10a) in a similar reaction gave derivatives of a novel ring system benzopyrano<3,2-d>pyrimidine (8) but when 3-amino-4-oxochromene-2-carboxamide (10b) was subjected to the same reaction, the novel ring system benzopyrano<3,2-e>-1,4-diazepine (14a) was obtained in high yield.This structure, which contains the hitherto unknown 1,4-diazepine-2,3,5-trione ring, is supported by spectroscopic and chemical evidence.The presence of a 3-amino and a 2-carbonyl group in a chromone has an unexpected shielding effect on the chemical shift of C-8.The course of the cyclization was studied.Attempts to cyclize 3-aminomethyl-4-oxochromene-2-carboxamide (28; X= Y= H), a homologue of (10b), failed but a new ring system (31) was obtained when ethyl 3-bromo-4-oxochromene-2-carboxylate (29; R1= OEt) reacted with o-phenylenediamine.

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Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N295 | ChemSpider

Synthetic Route of 2213-63-0, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2213-63-0, Name is 2,3-Dichloroquinoxaline, molecular formula is C8H4Cl2N2. In a Article£¬once mentioned of 2213-63-0

Synthesis, structural, catecholase, tyrosinase and DFT studies of pyrazoloquinoxaline derivatives

Six functional multidentate ligands: 2,3-bis(3,5-dimethyl-1H-pyrazol-1-yl) quinoxaline, L1, 2,3-bis(3,5-dimethyl-1H-pyrazol-1-yl)-6-nitroquinoxaline, L2, 2,3-bis(3,5-dimethyl-1H-pyrazol-1-yl)-6-methylquinoxaline, L3, 2-(3,5-dimethyl-1H-pyrazol-1-yl)-3-hydrazinyl-6-nitroquinoxaline L4, 2-chloro-3-(3,5-dimethyl-1H-pyrazol-1-yl)-6-methylquinoxaline, L5, 2-chloro-3-(3,5-dimethyl-1H-pyrazol-1-yl) quinoxaline, L6, and a new copper (II) complex, were prepared and evaluated for their catecholase activities at aerobic conditions. We found that, the reaction rate depends on: The nature of the substituents in the quinoxaline ring, counter anion, metal, concentration of ligand and the used solvent. The complex obtained in-situ from reaction of one equivalent of ligand L1 and two equivalents of Cu(CH3COO)2 in methanol showed the highest oxidation rate activity (V?=?33.48?mumol?L?1. min?1). In addition, geometry optimizations of the complexes in order to get better insight into the geometry and the electronic structure and chemical reactivity were carried out by means of DFT calculations.

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Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1277 | ChemSpider

Application of 18514-76-6, Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. 18514-76-6, Name is 5-Nitroquinoxaline,introducing its new discovery.

A aromatic ring [a] carbazole and synthetic method of compound (by machine translation)

The invention discloses a aromatic ring and [a] Carbazole compound synthesis method, which belongs to the technical field of organic synthesis. The technical scheme of the present invention to point is: connected to the 2 – phenyl indole compound, 2 – (naphthalene – 1 – yl) indole compounds or 2 – (thiazole – 1 – yl) indole compounds with the diazo compounds are dissolved in the solvent, then adding catalyst and additive, for 100 – 140 C reaction, to respectively obtain benzo [a] Carbazole compound, naphtho [a] Carbazole compound or imidazo [a] Carbazole compound. The invention relates to 2 – substituted indole compound and diazo compounds as raw materials, through the one-pot Serial reaction, aromatic ring and directly [a] Carbazole compound, synthetic process operation is convenient, mild condition, substrate and wide range of application, is suitable for industrial production. (by machine translation)

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Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N820 | ChemSpider