Tag: 120.15

Green catalytic pyrolysis: an eco-friendly route for the production of fuels and chemicals by blending oil industry wastes and waste furniture wood was written by Gift, M. D. Mohan;Verma, Savita;Prasad, Kalapala;Kathiresan, K.;Prasad, Rohi;Logeswaran, T.;Ghotekar, Suresh;Thao, D. V.;Lalvani, J. Isaac Joshua Ramesh. And the article was included in Journal of Nanomaterials in 2022.Product Details of 496-16-2 This article mentions the following:

Lignocellulosic biomass is converted into liquid products through pyrolysis, which can be used as an alternative fuel for heating applications and industrial chems. Pyrolysis liquid is a mixture of many oxygenated fractions which deteriorates its burning properties. Through specific bond cleavage reactions like deoxygenation, cracking, and decarbonylation, catalysts in the pyrolysis process can be used to improve the quality of pyrolysis liquid In this study, biochar produced by carbonization of printed circuit boards was used for catalytic reforming processes to produce energy-rich liquids and chems. from a mixture of karanja seed oil cake and waste furniture wood. The catalytic process was performed by changing the reactor temperature from 300°C to 700°C at 50°C intervals. The results showed a maximum liquid oil recovery of 53.9 wt% at 500°C. Compared to the noncatalytic reaction, pyrolysis of biomass with biochar recovered 11.59% more liquid This study demonstrated a viable technique to recover more liquid products and industrial chems. by employing sustainable catalysts from e-waste. The phys. anal. of the liquid showed that the liquid can be used as a fuel for boilers and furnaces. The chem. characterization through gas chromatog.-mass spectroscopy (GC-MS) showed the presence of various chem. elements used for medicinal and industrial applications. 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. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. 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.Product Details of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Rhodium-Catalyzed Benzylic Addition Reactions of Alkylarenes to Michael Acceptors was written by Li, Yuntong;Wu, Wen-Qiang;Zhu, Hui;Kang, Qi-Kai;Xu, Lun;Shi, Hang. And the article was included in Angewandte Chemie, International Edition in 2022.Name: 2,3-Dihydrobenzo[b]furan This article mentions the following:

Herein, Rh-catalyzed benzylic addition of alkylarenes to Michael acceptors for the formation of C(sp³)-C(sp³) bonds was reported. The catalyst was proposed to activate the aromatic ring via η⁶-coordination, dramatically facilitating deprotonation of the unactivated benzylic C-H bond and addition of the resulting carbanion to the α,β-unsaturated double bond in the absence of bases. Notably, this byproduct-free method provided an access to all-carbon quaternary centers through the development of ligands. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Name: 2,3-Dihydrobenzo[b]furan).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. 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.Name: 2,3-Dihydrobenzo[b]furan

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Molecular nanoinformatics approach assessing the biocompatibility of biogenic silver nanoparticles with channelized intrinsic steatosis and apoptosis was written by Panda, Pritam Kumar;Kumari, Puja;Patel, Paritosh;Samal, Shailesh Kumar;Mishra, Suman;Tambuwala, Murtaza M.;Dutt, Ateet;Hilscherova, Klara;Mishra, Yogendra Kumar;Varma, Rajender S.;Suar, Mrutyunjay;Ahuja, Rajeev;Verma, Suresh K.. And the article was included in Green Chemistry in 2022.Related Products of 496-16-2 This article mentions the following:

The developmental rapidity of nanotechnol. poses higher risks of exposure to humans and the environment through manufactured nanomaterials. The multitude of biol. interfaces, such as DNA, proteins, membranes, and cell organelles, which come in contact with nanoparticles, is influenced by colloidal and dynamic forces. Consequently, the ensued nano-bio interface depends on dynamic forces, encompasses many cellular absorption mechanisms along with various biocatalytic activities, and biocompatibility that needs to be investigated in detail. Addressing the issue, the study offers a novel green synthesis strategy for antibacterial AgNPs with higher biocompatibility and elucidates the mechanistic in vivo biocompatibility of silver nanoparticles (AgNPs) at the cellular and mol. levels. The anal. ascertained the biosynthesis of G-AgNPs with the size of 25 ± 10 nm and zeta potential of -29.2 ± 3.0 mV exhibiting LC50 of 47.2 μg mL-1 in embryonic zebrafish. It revealed the mechanism as a consequence of abnormal physiol. metabolism in oxidative stress and neutral lipid metabolism due to dose-dependent interaction with proteins such as he1a, sod1, PEX protein family, and tp53 involving amino acids such as arginine, glutamine and leucine leading to improper apoptosis. The research gave a detailed insight into the role of diverse AgNPs-protein interactions with a unique combinatorial approach from first-principles d. functional theory and in silico analyses, thus paving a new pathway to comprehending their intrinsic properties and usage. 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. 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. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Related Products of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Dynamic changes of volatile and phenolic components during the whole manufacturing process of Wuyi Rock tea (Rougui) was written by Liu, Zhibin;Chen, Fuchen;Sun, Jinyuan;Ni, Li. And the article was included in Food Chemistry in 2022.Safety of 2,3-Dihydrobenzo[b]furan This article mentions the following:

Wuyi Rock tea (WRT), a top-ranking oolong tea, possesses characteristic woody, floral, nutty flavor. WRT flavor is mainly formed during the manufacturing process. However, details regarding its formation process are not fully understood yet. In this study, the dynamics of volatile and phenolic components over the whole manufacturing process of WRT were investigated. During withering, despite minor changes in volatile and phenolic components, the central vacuole shrunk remarkably, which reduced the cell mech. performance and facilitated the subsequent enzymic fermentation During fermentation, approx. 78% of flavan-3-ols in fresh tea leaves were oxidized and converted to a diverse mixture of highly heterogeneous oxidation products, such as theaflavins, whereas flavonols, phenolic acids, and xanthine alkaloids remained stable throughout the manufacturing process. Aldehydes, ketones, and heterocyclic compounds, imparting woody, floral, and nutty scent, were mainly formed during the roasting steps. This detailed information can expand our understanding on the formation of WRT flavor. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Safety of 2,3-Dihydrobenzo[b]furan).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives.Benzofuran is one of the most significant oxygen-containing heterocycles consisting of fused benzene and furan ring, which are widely presented in various naturally occurring and synthetically active compounds. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Safety of 2,3-Dihydrobenzo[b]furan

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Green catalytic pyrolysis: an eco-friendly route for the production of fuels and chemicals by blending oil industry wastes and waste furniture wood was written by Gift, M. D. Mohan;Verma, Savita;Prasad, Kalapala;Kathiresan, K.;Prasad, Rohi;Logeswaran, T.;Ghotekar, Suresh;Thao, D. V.;Lalvani, J. Isaac Joshua Ramesh. And the article was included in Journal of Nanomaterials in 2022.Product Details of 496-16-2 This article mentions the following:

Lignocellulosic biomass is converted into liquid products through pyrolysis, which can be used as an alternative fuel for heating applications and industrial chems. Pyrolysis liquid is a mixture of many oxygenated fractions which deteriorates its burning properties. Through specific bond cleavage reactions like deoxygenation, cracking, and decarbonylation, catalysts in the pyrolysis process can be used to improve the quality of pyrolysis liquid In this study, biochar produced by carbonization of printed circuit boards was used for catalytic reforming processes to produce energy-rich liquids and chems. from a mixture of karanja seed oil cake and waste furniture wood. The catalytic process was performed by changing the reactor temperature from 300°C to 700°C at 50°C intervals. The results showed a maximum liquid oil recovery of 53.9 wt% at 500°C. Compared to the noncatalytic reaction, pyrolysis of biomass with biochar recovered 11.59% more liquid This study demonstrated a viable technique to recover more liquid products and industrial chems. by employing sustainable catalysts from e-waste. The phys. anal. of the liquid showed that the liquid can be used as a fuel for boilers and furnaces. The chem. characterization through gas chromatog.-mass spectroscopy (GC-MS) showed the presence of various chem. elements used for medicinal and industrial applications. 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. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. 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.Product Details of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Rhodium-Catalyzed Benzylic Addition Reactions of Alkylarenes to Michael Acceptors was written by Li, Yuntong;Wu, Wen-Qiang;Zhu, Hui;Kang, Qi-Kai;Xu, Lun;Shi, Hang. And the article was included in Angewandte Chemie, International Edition in 2022.Name: 2,3-Dihydrobenzo[b]furan This article mentions the following:

Herein, Rh-catalyzed benzylic addition of alkylarenes to Michael acceptors for the formation of C(sp³)-C(sp³) bonds was reported. The catalyst was proposed to activate the aromatic ring via η⁶-coordination, dramatically facilitating deprotonation of the unactivated benzylic C-H bond and addition of the resulting carbanion to the α,β-unsaturated double bond in the absence of bases. Notably, this byproduct-free method provided an access to all-carbon quaternary centers through the development of ligands. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Name: 2,3-Dihydrobenzo[b]furan).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives. Benzofuran is the “”parent”” of many related compounds with more complex structures. For example, psoralen is a benzofuran derivative that occurs in several plants. 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.Name: 2,3-Dihydrobenzo[b]furan

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Molecular nanoinformatics approach assessing the biocompatibility of biogenic silver nanoparticles with channelized intrinsic steatosis and apoptosis was written by Panda, Pritam Kumar;Kumari, Puja;Patel, Paritosh;Samal, Shailesh Kumar;Mishra, Suman;Tambuwala, Murtaza M.;Dutt, Ateet;Hilscherova, Klara;Mishra, Yogendra Kumar;Varma, Rajender S.;Suar, Mrutyunjay;Ahuja, Rajeev;Verma, Suresh K.. And the article was included in Green Chemistry in 2022.Related Products of 496-16-2 This article mentions the following:

The developmental rapidity of nanotechnol. poses higher risks of exposure to humans and the environment through manufactured nanomaterials. The multitude of biol. interfaces, such as DNA, proteins, membranes, and cell organelles, which come in contact with nanoparticles, is influenced by colloidal and dynamic forces. Consequently, the ensued nano-bio interface depends on dynamic forces, encompasses many cellular absorption mechanisms along with various biocatalytic activities, and biocompatibility that needs to be investigated in detail. Addressing the issue, the study offers a novel green synthesis strategy for antibacterial AgNPs with higher biocompatibility and elucidates the mechanistic in vivo biocompatibility of silver nanoparticles (AgNPs) at the cellular and mol. levels. The anal. ascertained the biosynthesis of G-AgNPs with the size of 25 ± 10 nm and zeta potential of -29.2 ± 3.0 mV exhibiting LC50 of 47.2 μg mL-1 in embryonic zebrafish. It revealed the mechanism as a consequence of abnormal physiol. metabolism in oxidative stress and neutral lipid metabolism due to dose-dependent interaction with proteins such as he1a, sod1, PEX protein family, and tp53 involving amino acids such as arginine, glutamine and leucine leading to improper apoptosis. The research gave a detailed insight into the role of diverse AgNPs-protein interactions with a unique combinatorial approach from first-principles d. functional theory and in silico analyses, thus paving a new pathway to comprehending their intrinsic properties and usage. 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. 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. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Related Products of 496-16-2

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem

Dynamic changes of volatile and phenolic components during the whole manufacturing process of Wuyi Rock tea (Rougui) was written by Liu, Zhibin;Chen, Fuchen;Sun, Jinyuan;Ni, Li. And the article was included in Food Chemistry in 2022.Safety of 2,3-Dihydrobenzo[b]furan This article mentions the following:

Wuyi Rock tea (WRT), a top-ranking oolong tea, possesses characteristic woody, floral, nutty flavor. WRT flavor is mainly formed during the manufacturing process. However, details regarding its formation process are not fully understood yet. In this study, the dynamics of volatile and phenolic components over the whole manufacturing process of WRT were investigated. During withering, despite minor changes in volatile and phenolic components, the central vacuole shrunk remarkably, which reduced the cell mech. performance and facilitated the subsequent enzymic fermentation During fermentation, approx. 78% of flavan-3-ols in fresh tea leaves were oxidized and converted to a diverse mixture of highly heterogeneous oxidation products, such as theaflavins, whereas flavonols, phenolic acids, and xanthine alkaloids remained stable throughout the manufacturing process. Aldehydes, ketones, and heterocyclic compounds, imparting woody, floral, and nutty scent, were mainly formed during the roasting steps. This detailed information can expand our understanding on the formation of WRT flavor. In the experiment, the researchers used many compounds, for example, 2,3-Dihydrobenzo[b]furan (cas: 496-16-2Safety of 2,3-Dihydrobenzo[b]furan).

2,3-Dihydrobenzo[b]furan (cas: 496-16-2) belongs to benzofurans derivatives.Benzofuran is one of the most significant oxygen-containing heterocycles consisting of fused benzene and furan ring, which are widely presented in various naturally occurring and synthetically active compounds. Substituted benzofurans find applications such as fluorescent sensors, oxidants, in drug discovery, and in another field of chemistry and agriculture.Safety of 2,3-Dihydrobenzo[b]furan

Referemce:
Benzofuran – Wikipedia,
Benzofuran | C8H6O – PubChem