Properties and Exciting Facts About 2-Methylbenzofuran

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4265-25-2, Name is 2-Methylbenzofuran, belongs to benzofuran compound, is a common compound. Computed Properties of C9H8OIn an article, once mentioned the new application about 4265-25-2.

Ruthenium NHC catalyzed highly asymmetric hydrogenation of benzofurans

H2-O-T! Aromatic O-heterocycles are a challenging substrates for asymmetric hydrogenation (H2). An in situ formed chiral N-heterocyclic carbene (NHC) ruthenium complex allows the high yielding, completely regioselective, and highly asymmetric hydrogenation of substituted benzofurans at room Temperature, giving valuable 2,3-dihydrobenzofurans (see scheme). Copyright

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Benzofuran – Wikipedia,
Benzofuran | C8H232O – PubChem

Properties and Exciting Facts About Thymolphthalein

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The Thermal Stability and Rheological Properties of Alkylated Carboxymethyl Starch

Several alkylated carboxymethyl starches (CMS) with different alkyl chain lengths were prepared. The influence of the number of alkyls on the thermal stability and rheological properties, such as thickening properties, salt-tolerance, temperature sensitivity and time-dependent rheological behavior, are discussed. The initial decomposition temperature (IDT) of alkylated CMS reached 263C ?293C which, as compared to the IDT for CMS itself (230C), indicated that the thermal stability of CMS was improved after being alkylated. The solution viscosities of the alkylated carboxymethyl starch increased with the increasing of alkyl length. With the alkyl chain length increasing from C2 to C8, the viscosity increased from 400?mPa¡¤s to 38000?mPa¡¤s. The weak hydrophobic aggregation of the alkyl groups did not improve the shear-resistance and relative hysteresis area. But the temperature sensitivity of alkylated CMS was improved as the chain length of the alkyl groups increased, as the activation energy (Ea) value decreased from 2.082?kJ¡¤mol?1 to 0.077?kJ¡¤mol?1; Improving the rigidity of the molecular chains and reducing the network structure of the hydrophobic contribution to the viscosity of the solution are benefits for improving the salt-tolerance and shear-resistance of the aqueous solution.

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Benzofuran – Wikipedia,
Benzofuran | C8H4431O – PubChem

Discovery of Thymolphthalein

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A calcium oxide-based catalyst derived from palm kernel shell gasification residues for biodiesel production

The fruit of oil-palm trees is used to extract millions of tons of palm oil annually across the globe. The extraction of palm oil leaves behind various residues such as empty fruit bunches, mill sludge and fibers, shells, and palm kernel cake. Considering the large amounts of solid organic wastes that are produced in oil palm mills, there is a need for their recovery and utilization. Palm kernel shells (PKS) are the most difficult fraction of the solid waste to decompose. In this work, PKS solid residues which had been subjected to thermal treatment in a gasifier were used as raw materials for the production of a calcium oxide (quicklime/burnt lime) catalyst. The produced catalyst was fully characterized by SEM-EDX, XRF, XRD, CHNS, TGA, and BET analyses. In addition, the basic strength and basicity of the catalyst were determined. The catalytic activity of the CaO-based catalyst was verified in transesterification of sunflower oil with methanol. The effect of the catalyst loading on the fatty acid methyl esters (FAME) formation at a methanol-to-sunflower oil ratio (9:1) at 60C was studied. The results show that the calcium carbonate contained in the palm kernel shell biochars is a promising source for calcium oxide catalyst production.

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Benzofuran – Wikipedia,
Benzofuran | C8H4267O – PubChem

Awesome and Easy Science Experiments about (2,3-Dihydrobenzofuran-6-yl)methanol

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Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. SDS of cas: 1083168-69-7. Introducing a new discovery about 1083168-69-7, Name is (2,3-Dihydrobenzofuran-6-yl)methanol

Orally active ghrelin receptor inverse agonists and their actions on a rat obesity model

A series of 2-alkylamino nicotinamide analogs was prepared as orally active ghrelin receptor (ghrelinR) inverse agonists. Starting from compound 1, oral bioavailability was improved by modifying metabolically unstable sites and reducing molecular weight. Brain-permeable compound 33 and compound 24 with low brain permeability were tested in rat models of obesity; 30 mg/kg of compound 33 suppressed weight gain. PK/PD analysis revealed that the anti-obesity effect of ghrelinR inverse agonists depends on their brain concentrations.

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Benzofuran – Wikipedia,
Benzofuran | C8H1521O – PubChem

Extended knowledge of 1552-42-7

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Fabrication and characterization of reversible thermochromic wood veneers

Leuco dyes are widely used as functional materials for their thermosensitive chromogenic nature. The influences of thermochromic compounds and impregnation processing conditions on thermochromic wood veneer properties were investigated in this paper. The thermochromic compounds included thermochromic dye (ODB-2), color developer (bisphenol A) and solvent (1-tetradecanol). To achieve the maximum color change, the optimum mixing ratio of ODB-2 to bisphenol A to 1-tetradecanol was 1:2:60. Juglans mandshurica veneers were ultrasonically impregnated with reversible thermochromic compound suspensions. Analysis of variance showed that the influences of impregnation parameters on veneer color change were significant at the 0.05 level. The optimum thermochromic wood veneer can be obtained by impregnating with a thermochromic compound suspension for 2.0 min at 65 C. In this paper, the thermochromic properties of wood veneers were evaluated, and functional thermochromic veneers exhibited excellent properties and thermostability.

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Benzofuran – Wikipedia,
Benzofuran | C8H4222O – PubChem

The important role of 4265-25-2

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Aroma profile of rice varieties by a novel SPME method able to maximize 2-acetyl-1-pyrroline and minimize hexanal extraction

The solid phase microextraction (SPME) has been the most used technique for the extraction of volatile compounds from rice because of its easy operation and solvent-free. The extraction parameters, sample mass and incubation temperature, were optimized through a central composite rotational design (CCRD), aiming at maximizing the extraction of 2-acetyl-1-pyrroline (2AP), the main compound responsible for the aroma in aromatic rice, and minimizing the generation of hexanal, a marker of lipid oxidation. Besides, the time of sample incubation and fiber exposure for the extraction of the volatile compounds from rice were determined. The optimized conditions for SPME were: 2.5 g of ground rice in a 20 mL vial, sample incubation at 80 C for 60 min and exposure of the divinylbenzene/carboxene/polydimethylsiloxane (DVB/CAR/PDMS) fiber in the headspace for 10 min. The optimized method was sucessfuly applied to 12 varieties of rice and principal component analysis (PCA) was performed to observe similarities in their volatile profile. A total of 152 volatile compounds were identified among the different rice varieties. From these, 42 were identified in arborio rice, 47 in basmati brand A, 43 in basmati brand B, 55 in black rice, 63 in brown rice, 39 in jamine rice, 50 in parboiled brown rice, 43 in parboiled rice, 54 in red rice, 63 in sasanishiki rice, 46 in white rice and 70 in wild rice.

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Benzofuran – Wikipedia,
Benzofuran | C8H89O – PubChem

Top Picks: new discover of 5-Methoxyisobenzofuran-1(3H)-one

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Application of 4741-62-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.4741-62-2, Name is 5-Methoxyisobenzofuran-1(3H)-one, molecular formula is C9H8O3. In a article£¬once mentioned of 4741-62-2

Site-Selective Functionalization of (sp3)C?H Bonds Catalyzed by Artificial Metalloenzymes Containing an Iridium-Porphyrin Cofactor

The selective functionalization of one C?H bond over others in nearly identical steric and electronic environments can facilitate the construction of complex molecules. We report site-selective functionalizations of C?H bonds, differentiated solely by remote substituents, catalyzed by artificial metalloenzymes (ArMs) that are generated from the combination of an evolvable P450 scaffold and an iridium-porphyrin cofactor. The generated systems catalyze the insertion of carbenes into the C?H bonds of a range of phthalan derivatives containing substituents that render the two methylene positions in each phthalan inequivalent. These reactions occur with site-selectivity ratios of up to 17.8:1 and, in most cases, with pairs of enzyme mutants that preferentially form each of the two constitutional isomers. This study demonstrates the potential of abiotic reactions catalyzed by metalloenzymes to functionalize C?H bonds with site selectivity that is difficult to achieve with small-molecule catalysts.

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Benzofuran – Wikipedia,
Benzofuran | C8H2260O – PubChem

Extended knowledge of Ethyl (5-bromobenzofuran)-2-carboxylate

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Electrochemically Driven, Ni-Catalyzed Aryl Amination: Scope, Mechanism, and Applications

C-N cross-coupling is one of the most valuable and widespread transformations in organic synthesis. Largely dominated by Pd- and Cu-based catalytic systems, it has proven to be a staple transformation for those in both academia and industry. The current study presents the development and mechanistic understanding of an electrochemically driven, Ni-catalyzed method for achieving this reaction of high strategic importance. Through a series of electrochemical, computational, kinetic, and empirical experiments, the key mechanistic features of this reaction have been unraveled, leading to a second generation set of conditions that is applicable to a broad range of aryl halides and amine nucleophiles including complex examples on oligopeptides, medicinally relevant heterocycles, natural products, and sugars. Full disclosure of the current limitations and procedures for both batch and flow scale-ups (100 g) are also described.

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Benzofuran – Wikipedia,
Benzofuran | C8H4045O – PubChem

Archives for Chemistry Experiments of Benzofuran-2-carboxylic acid

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Rhodium-catalyzed C3-selective alkenylation of substituted thiophene-2-carboxylic acids and related compounds

The regioselective C3-alkenylation of thiophene-2-carboxylic acids can be achieved effectively via rhodium/silver-catalyzed oxidative coupling with alkenes, unaccompanied by decarboxylation. A wide range of substrates including brominated thiophenecarboxylic acids and furan-2-carboxylic acids can be employed together with styrenes as well as acrylates. The present catalyst system is also applicable to ortho-alkenylation of benzoic acids.

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Benzofuran – Wikipedia,
Benzofuran | C8H1830O – PubChem

Some scientific research about 35700-40-4

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Tomato stress-responsive factor TSRF1 interacts with ethylene responsive element GCC box and regulates pathogen resistance to Ralstonia solanacearum

Ethylene responsive factors (ERFs) are important in regulating plant pathogen resistance, abiotic stress tolerance and plant development. Recent studies have greatly enlarged the ERF protein family and revealed more important roles of ERFs in plants. Here, we report our finding of a tomato ERF protein TSRF1, which is transcriptionally up-regulated by ethylene, salicylic acid, or Ralstonia solanacearum strain BJ1057 infection. Biochemical analysis indicates that TSRF1 specifically interacts in vitro with the GCC box, an element present in the promoters of many pathogenesis-related (PR) genes. Further investigation evidences that TSRF1 activates in vivo the expression of reporter beta-glucuronidase gene controlled by GCC box. More importantly, overexpressing TSRF1 in tobacco and tomato constitutively activates the expression of PR genes, and subsequently enhancing transgenic plant resistance to the bacterial wilt caused by Ralstonia solanacearum strain BJ1057. Therefore our investigation not only extends the functions of ERF proteins in plant resistance to R. solanacearum, but also provides further clues to understanding the mechanism of host regulatory proteins in response to the infection of pathogens.

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Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H2215O – PubChem