Jiang, Liyang et al. published their research in Fuel in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans are stable towards alkali and readily polymerize on treatment with sulfuric acid, due to which they are useful for the preparation of low cost chemically relatively inert resins.Product Details of 496-16-2

Characteristics and synergistic effects of co-pyrolysis of microalgae with polypropylene was written by Jiang, Liyang;Zhou, Zhen;Xiang, Huan;Yang, Yang;Tian, Hong;Wang, Jiawei. And the article was included in Fuel in 2022.Product Details of 496-16-2 This article mentions the following:

To further improve the quality of microalgae-derived bio-oil, the characteristics, kinetic parameters and product distribution of the co-pyrolysis of polypropylene (PP) and Chlorella vulgaris (C.V) were studied by thermogravimetric anal. (TGA) and pyrolysis gas chromatog./mass spectrometry (Py-GC/MS). The TGA results showed that with the increase of the PP amount, the peak temperature of maximum pyrolysis weight loss of C. V decreased, but the trend of PP was opposite. Compared with the exptl. and theor. values, it was found that the residual amount of solid coke and the total activation energy required for co-pyrolysis were significantly reduced, which indicated that there was an obvious synergistic effect during the co-pyrolysis process. The Py-GC/MS results showed that when the PP mass ratio was 0.75 and the final pyrolysis temperature was 500°C, the reaction activation energy and hydrocarbon yield had the best synergistic effect. Moreover, the co-pyrolysis of C. V and PP promoted the formation of aliphatic hydrocarbons, inhibited the aromatisation and Maillard reactions, and hindered the formation of aromatics, nitrogenous compounds, acids and oxides. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Product Details of 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans are stable towards alkali and readily polymerize on treatment with sulfuric acid, due to which they are useful for the preparation of low cost chemically relatively inert resins.Product Details of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Liu, Yang-Yang et al. published their research in Catalysis Science & Technology in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives have shown many biological activities, including antifungal and antimicrobial properties, and acting as antagonists of H3 receptors and angiotensin II. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.COA of Formula: C8H8O

Generation of local redox potential from confined nano-bimetals in porous metal silicate materials for high-performance catalysis was written by Liu, Yang-Yang;Shi, Xiao-Ke;Wu, Chuan-De. And the article was included in Catalysis Science & Technology in 2022.COA of Formula: C8H8O This article mentions the following:

Partial hydrogenation of polycyclic aromatic hydrocarbons (PAHs) could not only produce highly value-added chems. but also reduce environmental pollution; however, the partial hydrogenation reaction has to be performed under extreme conditions in the presence of precious metal-based catalysts, because PAHs are a class of inactive reactants. We report herein a porous metal silicate (PMS) material, PMS-16, that consists of Co and Ni bimetal redox-active species and BIII Lewis acid sites, demonstrating high catalytic activity (>99% conversion) and selectivity (>99%) for hydrogenation of a series of PAHs under mild conditions, which is much superior to noble metal-based catalysts in the literature. The unique catalytic properties of PMS-16 are derived from the synergistic work between Ni and Co metal species by sep. activating different reactant mols. and generating local redox potential to prompt electron and charge transfer. The catalyst is simply produced and very stable for industrial applications. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2COA of Formula: C8H8O).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives have shown many biological activities, including antifungal and antimicrobial properties, and acting as antagonists of H3 receptors and angiotensin II. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.COA of Formula: C8H8O

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Silva, Mariana P. et al. published their research in Journal of Analytical and Applied Pyrolysis in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives have shown many biological activities, including antifungal and antimicrobial properties, and acting as antagonists of H3 receptors and angiotensin II. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.Related Products of 496-16-2

Valuable chemicals identified from Flourensia species using vacuum and analytical pyrolysis was written by Silva, Mariana P.;Nieva Lobos, Maria L.;Larson, Tony R.;McQueen-Mason, Simon;Gomez, Leonardo D.;Moyano, E. Laura;Scopel, Ana L.. And the article was included in Journal of Analytical and Applied Pyrolysis in 2022.Related Products of 496-16-2 This article mentions the following:

The genus Flourensia, present throughout most of the Americas has been identified as a source of renewable chems. Here, we characterized the aerial biomass and matrix polysaccharides of Flourensia campestris, F. oolepis and F. riparia, and explored their potential as a source of chems. through the study of two techniques: anal. pyrolysis (PY-GC/MS) and vacuum pyrolysis (VP). In all species, hemicellulose was more abundant than cellulose and lignin, with galacturonic acid being the most abundant monosaccharide. Bio-oils from VP exhibited a complex combination of phenols, terpenes, furans and nitrogen-containing compounds which have a wide range of industrial applications. Differences between the composition of VP pyrolytic oils derived from the mixture of leaves and stems or from individual organs suggest possible interactions between biopolymers. Combining PY-GC/MS and principal component anal. (PCA) we identified fingerprints for leaves and stems of the three Flourensia species. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Related Products of 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives have shown many biological activities, including antifungal and antimicrobial properties, and acting as antagonists of H3 receptors and angiotensin II. Introduction of benzofurans in organic synthesis, particularly drug synthesis, involves generally the use of their metalated species as nucleophiles in addition reactions or in metal-catalysed cross-coupling reactions.Related Products of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Ito, Tasuku et al. published their research in Journal of Organic Chemistry in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. In nature, benzofurans have occupied an important role among the plant phenols & several pharmacologically active compounds.SDS of cas: 496-16-2

TEMPO as a Hydrogen Atom Transfer Catalyst for Aerobic Dehydrogenation of Activated Alkanes to Alkenes was written by Ito, Tasuku;Seidel, Falk William;Jin, Xiongjie;Nozaki, Kyoko. And the article was included in Journal of Organic Chemistry in 2022.SDS of cas: 496-16-2 This article mentions the following:

2,2,6,6-Tetramethylpiperidine-N-oxyl (TEMPO) has been extensively utilized as a radical scavenger or an oxidation catalyst. In contrast, TEMPO as a hydrogen atom transfer (HAT) catalyst has rarely been studied. Here, authors report that TEMPO, as the HAT catalyst, homolytically cleaves benzylic or allylic C-H bonds to give the corresponding alkyl radicals. Benefiting from the dual roles played by TEMPO as the HAT catalyst and the radical scavenger, the highly challenging aerobic dehydrogenation of activated alkanes to alkenes is successfully developed. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2SDS of cas: 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran is a core structural unit found in many naturally occurring compounds with multidirectional biological activities. In nature, benzofurans have occupied an important role among the plant phenols & several pharmacologically active compounds.SDS of cas: 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Gao, Hui et al. published their research in Organic Chemistry Frontiers in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. They are also prone to polymerisation in the presence of concentrated mineral acids and Lewis acids.SDS of cas: 496-16-2

Electrochemical benzylic C-H arylation of xanthenes and thioxanthenes without a catalyst and oxidant was written by Gao, Hui;Chen, Xinyu;Wang, Pei-Long;Shi, Meng-Meng;Shang, Ling-Long;Guo, Heng-Yi;Li, Hongji;Li, Pinhua. And the article was included in Organic Chemistry Frontiers in 2022.SDS of cas: 496-16-2 This article mentions the following:

A catalyst-free and oxidant-free C-H arylation of xanthenes and thioxanthenes I (R1 = H, Me, OH, Cl, etc.; R2 = H, OMe; R3R4 = -CH=CH-CH=CH-; X = O, S) using electrochem. has been developed, which affords a number of cross-coupling products II (R5 = 4-methoxyphenyl, 4-methoxy-3-methylphenyl, 4-methoxy-3,5-dimethylphenyl, 2H-1,3-benzodioxol-5-yl, etc.) in moderate to good yields. This method is atom- and step-economical as it uses cheap and easily available arenes and heteroarenes as partners directly and the C(sp2)-H/C(sp3)-H type cross-coupling reaction. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2SDS of cas: 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. They are also prone to polymerisation in the presence of concentrated mineral acids and Lewis acids.SDS of cas: 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Ling, Meiqi et al. published their research in Thermochimica Acta in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Recommanded Product: 496-16-2

Synthesis and pyrolysis mechanism of phenolphthalein poly(aryl ether sulfone) containing isopropyl groups was written by Ling, Meiqi;Yu, Kaifeng;Wang, Jian;Wang, Honghua;Nie, Heran;Wang, Zhipeng;Zhou, Guangyuan. And the article was included in Thermochimica Acta in 2022.Recommanded Product: 496-16-2 This article mentions the following:

A novel phenolphthalein poly(aryl ether sulfone) polymer containing iso-Pr groups (iPrPESC) has been successfully synthesized by SN2 aromatic nucleophilic polycondensation reaction. The pyrolysis mechanism and behavior of iPrPESC were investigated by thermogravimetry coupled with Fourier transform IR spectroscopy and pyrolysis combined with gas chromatog./mass spectrometry. TG-FTIR and Py-GC/MS were used to identify the thermal decomposition products and to determine the possible thermal degradation mechanism. The main mechanism for iPrPESC was one-stage pyrolysis involving main-chain random scission, and the major products of SO2 and phenol were released from the sulfone and ether groups in iPrPESC. The thermal degradation activation energy of iPrPESC was calculated to be 151 ± 4 and 139 ± 4 kJ mol-1 by the Flynn-Wall-Ozawa and Kissinger methods, resp., which were much lower than that of phenolphthalein poly(aryl ether sulfone). Furthermore, introduction of iso-Pr groups on the main chain can significantly reduce the char yield. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Recommanded Product: 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Recommanded Product: 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Sobek, S. et al. published their research in Renewable Energy in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Benzofurans are stable towards alkali and readily polymerize on treatment with sulfuric acid, due to which they are useful for the preparation of low cost chemically relatively inert resins.Application of 496-16-2

Brewer’s spent grain pyrolysis kinetics and evolved gas analysis for the sustainable phenolic compounds and fatty acids recovery potential was written by Sobek, S.;Zeng, K.;Werle, S.;Junga, R.;Sajdak, M.. And the article was included in Renewable Energy in 2022.Application of 496-16-2 This article mentions the following:

Within the presented paper, a thermochem. conversion via pyrolysis of spent grain from the local brewery (Alternatywa, Ruda Slaska, Poland) for phenolic compounds and fatty acids recovery is presented. Thermogravimetric pyrolysis was carried out at non-isothermal conditions (1, 2, and 4 K/min), under an inert N2 atmosphere. Deconvolution procedure for the kinetic modeling was implemented using own algorithm based on Gaussian function, using 3-stage kinetic mechanism, ascribed to the independent decomposition of the pseudo-components i.e., hemicellulose, cellulose, and bulk lignin-extractives. Released volatiles during pyrolysis was evaluated and recognized using gas chromatog.-mass spectrometry and Fourier-transform IR spectroscopy anal., which confirmed the high content of fatty acids, phenolic compounds, and nitrogen compounds, with shares of 23.95%, 13.94%, and 25.10% resp. Linkage of the desired product formations to the modeled kinetic stages of the BSG pyrolysis is a complex subject, and it is encouraged for future studies. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Application of 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran derivatives are one of the most important oxygen-containing heterocycles. Benzofurans are stable towards alkali and readily polymerize on treatment with sulfuric acid, due to which they are useful for the preparation of low cost chemically relatively inert resins.Application of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Yamakawa, Yuki et al. published their research in Journal of Organic Chemistry in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Quality Control of 2,3-Dihydrobenzo[b]furan

Iridium(III)-Catalyzed Asymmetric Site-Selective Carbene C-H Insertion during Late-Stage Transformation was written by Yamakawa, Yuki;Ikuta, Takashi;Hayashi, Hiroki;Hashimoto, Keigo;Fujii, Ryoma;Kawashima, Kyohei;Mori, Seiji;Uchida, Tatsuya;Katsuki, Tsutomu. And the article was included in Journal of Organic Chemistry in 2022.Quality Control of 2,3-Dihydrobenzo[b]furan This article mentions the following:

Here, it was observed that the iridium-salen complex 6 exhibited efficient catalysis in asym. carbene C-H insertion reactions. Under optimized conditions, benzylic, allylic, and propargylic C-H bonds e.g., I were converted to desired C-C bond products e.g., II in an excellent stereoselective manner. Excellent regioselectivity was demonstrated in the reaction using not only simple substrate but also natural products, bearing multiple reaction sites. Moreover, based on the mechanistic studies, the iridium-catalyzed unique C-H insertion reaction involved rate-determining asynchronous concerted processes. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Quality Control of 2,3-Dihydrobenzo[b]furan).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Quality Control of 2,3-Dihydrobenzo[b]furan

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Yamakawa, Yuki et al. published their research in Journal of Organic Chemistry in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Quality Control of 2,3-Dihydrobenzo[b]furan

Iridium(III)-Catalyzed Asymmetric Site-Selective Carbene C-H Insertion during Late-Stage Transformation was written by Yamakawa, Yuki;Ikuta, Takashi;Hayashi, Hiroki;Hashimoto, Keigo;Fujii, Ryoma;Kawashima, Kyohei;Mori, Seiji;Uchida, Tatsuya;Katsuki, Tsutomu. And the article was included in Journal of Organic Chemistry in 2022.Quality Control of 2,3-Dihydrobenzo[b]furan This article mentions the following:

Here, it was observed that the iridium-salen complex 6 exhibited efficient catalysis in asym. carbene C-H insertion reactions. Under optimized conditions, benzylic, allylic, and propargylic C-H bonds e.g., I were converted to desired C-C bond products e.g., II in an excellent stereoselective manner. Excellent regioselectivity was demonstrated in the reaction using not only simple substrate but also natural products, bearing multiple reaction sites. Moreover, based on the mechanistic studies, the iridium-catalyzed unique C-H insertion reaction involved rate-determining asynchronous concerted processes. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Quality Control of 2,3-Dihydrobenzo[b]furan).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are compounds with a planar structure having 10 pi electrons that include the lone pair on oxygen atom, which makes it more susceptible to electrophilic attack. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Quality Control of 2,3-Dihydrobenzo[b]furan

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Wang, Ruikun et al. published their research in Carbon in 2022 | CAS: 496-16-2

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Product Details of 496-16-2

Forming mechanism of coke microparticles from polymerization of aqueous organics during hydrothermal carbonization process of biomass was written by Wang, Ruikun;Jia, Jiandong;Jin, Qingzhuang;Chen, Hongwei;Liu, Hantao;Yin, Qianqian;Zhao, Zhenghui. And the article was included in Carbon in 2022.Product Details of 496-16-2 This article mentions the following:

Corn stalk was selected as a typical biomass, and the growth mechanism of coke microparticles was studied. The coke microparticles that formed from through the polymerization of aqueous organics during the hydrothermal carbonization (HTC) showed a considerable effect on the mass yield and physicochem. properties of the hydrochar. Results indicated that the average particle size of the coke microparticles rapidly increased to 6.25μm within the initial 2 h of HTC. The lower C/O at. ratio of the surface layer of the coke microparticles than that of the core, suggested that the core had a higher carbonization degree than the shell. On the basis of various measurements, the coke microparticles were inferred to have formed through the two stages of micronuclei formation and growth. Dissolved organics, including furfurals, furans, and phenols polymerized each other into aromatized macromols., and then formed solid-phase micronuclei. Subsequently, the oxygen containing groups of the micronuclei formed bonded with aqueous organic mols., as a result, the micronuclei grew up into coke microparticles. Meanwhile, the carbonization degree of the coke microparticles was enhanced due to continuous intra- and inter-mol. dehydration and decarboxylation reactions occurred between hydroxyl and carboxyl groups. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Product Details of 496-16-2).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofurans are only weakly aromatic in nature and they are cleaved by many oxidative and reductive conditions. Benzofurans have also made significant and distinctive contributions to biology. They exhibit several biological activities that range from antioxidant, antitubercular, antiplasmodial, insecticidal.Product Details of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem