Category: 100-19-6

An article Efficient aerobic oxidation of ethylbenzene accelerated by cu species in hydrotalcite WOS:000600589400004 published article about PHASE SELECTIVE OXIDATION; METAL-ORGANIC FRAMEWORK; 1 ATM; N-HYDROXYPHTHALIMIDE; CATALYTIC-OXIDATION; ACETOPHENONE; SYSTEM; ALKYLAROMATICS; COMPLEX; KETONES in [Dai, Xuan; Li, Xingyan; Tang, Shuangling; Peng, Xinhua] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China; [Zheng, Xuegen; Jiang, Ou] Sinopec Anqing Petrochem Co, Anqing 246000, Peoples R China in 2021.0, Cited 35.0. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

The simply prepared CuMgAl hydrotalcite (CuMgAl-LDH) has been developed as an efficient catalyst for the aerobic oxidation of ethylbenzene to acetophenone in the presence of N-Hydroxyphthalimide (NHPI). Various alkyl arenes could be tolerated under the selected reaction conditions. The kinetic study showed that the oxidation of ethylbenzene is a first-order reaction over CuMgAl-LDH. The mechanism study indicated that CuMgAl-LDH could accelerate not only the conversion of ethylbenzene, but also the transformation of the alcohol intermediate to ketone. The positive effect of surface basicity of the catalyst on the reaction has been observed in the aerobic oxidation of the ethylbenzene.

Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Dai, X; Li, XY; Tang, SL; Peng, XH; Zheng, XG; Jiang, O or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Recently I am researching about ENANTIOSELECTIVE SYNTHESIS; TRANSFER HYDROGENATION; ALIPHATIC-KETONES; SILICON-COMPOUNDS; PENTACOORDINATE; REAGENTS; PHOSPHORUS; REACTIVITY; COMPLEXES, Saw an article supported by the Northern Illinois University; Ryerson University. Name: 1-(4-Nitrophenyl)ethanone. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Skrypai, V; Varjosaari, SE; Azam, F; Gilbert, TM; Adler, MJ. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The asymmetric direct reductive amination of prochiral ketones with aryl amines using 1-hydrosilatrane with a chiral Bronsted acid catalyst is reported. This is the first known example of chiral Bronsted acid-catalyzed asymmetric reductive amination using a silane as the hydride source. The reaction features a highly practical reducing reagent and proceeds efficiently at room temperature without a specialized reaction setup or equipment to exclude air or moisture. This method provides high conversion and enantiomeric excess up to 84% of the desired chiral secondary amines with minimal side products.

Welcome to talk about 100-19-6, If you have any questions, you can contact Skrypai, V; Varjosaari, SE; Azam, F; Gilbert, TM; Adler, MJ or send Email.. Name: 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Rhodium(III)-Catalyzed Oxidative Annulation of Ketoximes with Sulfonamide: A Direct Approach to Indazoles WOS:000456633000004 published article about AZOBENZENES; AMIDATION; 1H-INDAZOLES; CYCLIZATION; ACCESS; AZIDES in [Wang, Ning; Liu, Lingling; Xu, Wentao; Zhang, Mengye; Huang, Zhibin; Shi, Daqing; Zhao, Yingsheng] Soochow Unvers, Coll Chem & Chem Engn, Key Lab Organ Synth Jiangsu Prov, 199 Renai St, Suzhou 215123, Jiangsu, Peoples R China in 2019.0, Cited 30.0. Name: 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A rhodium(III)-catalyzed intermolecular C-H amination of ketoxime and iodobenzene diacetate-enabled N-N bond formation in the synthesis of indazoles has been developed. A variety of functional groups were well tolerated, providing the corresponding products in moderate to good yields. Moreover, the nitro-substituted ketoximes are well compatible in this reaction, leading to the corresponding products in moderate to good yields.

Name: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Wang, N; Liu, LL; Xu, WT; Zhang, MY; Huang, ZB; Shi, DQ; Zhao, YS or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

I found the field of Chemistry very interesting. Saw the article Novel thiazole-piperazine derivatives as potential cholinesterase inhibitors published in 2019.0. Safety of 1-(4-Nitrophenyl)ethanone, Reprint Addresses Yurttas, L (corresponding author), Anadolu Univ, Fac Pharm, Dept Pharmaceut Chem, TR-26470 Eskisehir, Turkey.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Dementia is a cognitive disorder mostly associated with Alzheimer’s disease (AD) in addition to being seen in many other diseases of the central nervous system (CNS). The limited number of drugs is not sufficient to provide adequate improvement to increase the quality of life of patients suffering from this symptom; therefore, all treatment options should be evaluated in detail. In this study, new molecules, [2-(4-(2/3/4-substituted phenyl)piperazin-1-yl)-4-phenylthiazol-5-yl][3/4-substituted phenyl]methanone derivatives (1-44), were obtained and analyzed in terms of their anticholinesterase activities. Kinetic mode and molecular interactions were also evaluated. An enzyme inhibition study was undertaken on acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) using the Ellman method. Maestro program was used in molecular modeling studies. Forty-four compounds were evaluated on AChE and BChE enzymes at 10(-3) and 10(-4) concentrations. The inhibition concentrations were calculated as 0.268 mu M to 2.104 mu M for six compounds (4, 5, 16, 27, 37, and 38) on AChE. Compound 5 including the 4-methoxy substituent (IC50: 0.268 mu M) and compound 38 containing the 4-methoxy and 3-methyl substituents (IC50: 0.286 mu M) showed the highest AChE inhibitory activity. They were further examined in terms of hydrogen bonding with Arg296 and Ar-Ar interaction with Trp286. The activity of compound 5 was also assessed in mixed-type kinetic mode.

Safety of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Demirayak, S; Sahin, Z; Ertas, M; Bulbul, EF; Bender, C; Biltekin, SN; Berk, B; Saglik, BN; Levent, S; Yurttas, L or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Sadjadi, S; Akbari, M; Heravi, MM in AMER CHEMICAL SOC published article about HETEROGENEOUS CATALYST; NITROBENZENE HYDROGENATION; FUNCTIONALIZED HALLOYSITE; PLATINUM CATALYST; PD NANOPARTICLES; CLAY NANOTUBES; SUPPORTS; RAMAN; NANOCATALYSTS; PRECURSOR in [Sadjadi, Samahe] Iran Polymer & Petrochem Inst, Fac Petrochem, Gas Convers Dept, Tehran 1497713115, Iran; [Akbari, Maryam; Heravi, Majid M.] Alzahra Univ, Sch Sci, Dept Chem, Tehran 1993891176, Iran in 2019.0, Cited 58.0. Application In Synthesis of 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A novel nitrile-/cyano-free ionic liquid was synthesized and carbonized under two different carbonization methods in the presence of ZnCl2 as a catalyst to afford N-doped carbon materials. It was found that the carbonization condition could affect the nature and textural properties of the resulting carbon. In the following, ionic liquid-derived carbon was hybridized with naturally occurring halloysite nanotubes via two procedures, that is, hydrothermal treatment of halloysite and as-prepared carbon and carbonization of ionic liquid in the presence of halloysite. The two novel nanocomposites were then used for stabilizing Pd nanoparticles. Examining the structures and catalytic activities of the resulting catalysts for the hydrogenation of nitroarenes in aqueous media showed that the carbonization procedure and hybridization method could affect the structure and the catalytic activity of the catalysts and hydrothermal approach, in which the structure of halloysite is preserved, leading to the catalyst with superior catalytic activity.

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

COA of Formula: C8H7NO3. In 2020.0 ACS CATAL published article about NITROGEN-DOPED CARBON; SINGLE-ATOM CATALYST; METAL-ORGANIC FRAMEWORK; HIGHLY-EFFICIENT; SELECTIVE HYDROGENATION; POROUS CARBON; AQUEOUS-PHASE; REDUCTION; VANILLIN; GRAPHENE in [Zhang, Longkang; Shang, Ningzhao; Gao, Shutao; Wang, Junmin; Meng, Tao; Wu, Qiuhua; Wang, Chun; Wang, Zhi] Hebei Agr Univ, Coll Sci, Baoding 071001, Peoples R China; [Qiao, Yuqing] Yanshan Univ, Coll Environm & Chem Engn, Qinhuangdao 066004, Hebei, Peoples R China; [Wang, Haijun; Gao, Yongjun] Hebei Univ, Coll Chem & Environm Sci, Baoding 071000, Peoples R China; [Du, Congcong; Shen, Tongde; Huang, Jianyu] Yanshan Univ, Clean Nano Energy Ctr, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Hebei, Peoples R China in 2020.0, Cited 74.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Single-atom catalysts (SACS) have attracted much attention due to their outstanding catalytic performance in heterogeneous catalysis. Here, we report a template sacrificial method to fabricate an atomically dispersed Co catalyst; three C kinds of silica templates with different microstructures (MCM-41, SBA-15, and FDU-12) were employed and the effect of pore structure of the templates on the dispersity of Co was investigated. The catalysts fabricated with different templates presented different Co dispersities, leading to distinguishing catalytic performance. The optimized Co-1@NC-(SBA) catalyst with atomically dispersed Co displayed outstanding catalytic activity for the hydrodeoxygenation (HDO) of lignin-derived species as well as the hydrogenation of various nitroaromatics. The reaction mechanism of the HDO of vanillin was investigated by using density functional theory calculations as well.

COA of Formula: C8H7NO3. Welcome to talk about 100-19-6, If you have any questions, you can contact Zhang, LK; Shang, NZ; Gao, ST; Wang, JM; Meng, T; Du, CC; Shen, TD; Huang, JY; Wu, QH; Wang, HJ; Qiao, YQ; Wang, C; Gao, YJ; Wang, Z or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

HPLC of Formula: C8H7NO3. Recently I am researching about N-HETEROCYCLIC CARBENES; MOLECULAR-ORBITAL METHODS; GAUSSIAN-TYPE BASIS; CATALYTIC-HYDROGENATION; RUTHENIUM(II) COMPLEXES; IRIDIUM(III) COMPLEXES; PINCER LIGANDS; BOND FORMATION; COORDINATION CHEMISTRY; BASIS-SET, Saw an article supported by the Spanish Ministerio de Ciencia, Innovacion y Universidades [CTQ2015-69568-P, CTQ2016-75193-P, CTQ2016-80814-R, CTQ2016-81797-REDC]; Fundacion SenecaFundacion Seneca [19890/GERM/15]; Junta de AndaluciaJunta de Andalucia [PY18-3208]; SECITI-DF; CONACyT MexicoConsejo Nacional de Ciencia y Tecnologia (CONACyT) [263719]. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Hernndez-Jurez, M; Snchez, P; Lpez-Serrano, J; Lara, P; Gonzlez-Herrero, P; Rendn, N; Alvarez, E; Paneque, M; Surez, A. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The iridium complex1based on a metalated CNP ligand containing an imidazolin-2-ylidene fragment has been prepared by treatment of the ligand precursor4with Ag2O followed by reaction with [IrCl(COE)(2)](2). The chlorohydride imidazolidin-2-ylidene complex6, which is isostructural to1, was synthetized by reaction of the previously reported dihydride derivative3with CH2Cl2. Complexes1and6exhibit luminescence arising from a(3)MLCT/ILCT state involving the metalated CNP ligand, which is particularly intense for1in the solid state at 298 K. Furthermore, the reactivity of complexes1and6towards bases was compared. Deprotonation of1with KOtBu produced the selective formation of the dinuclear complex7; meanwhile, the reaction of6led to a complex mixture of products. The same reactions carried out in the presence of PPh(3)produced the selective deprotonation of the P-bonded methylene bridges of1and6, yielding the isostructural derivatives9and10. DFT calculations performed on theuNHC-containing tautomersIandII, and thesNHC-based isomersIIIandIV, showed that the NHC-deprotonated derivativesIIandIVare more stable by 3.20 and 2.73 kcal mol(-1), respectively, than their P-deprotonated counterparts (IandIII). However, a reverse stability order was observed for hexacoordinated tautomersI center dot LandII center dot L, andIII center dot LandIV center dot L(L = PPh3, CO, MeCN). Finally, the catalytic activity of complex3in the transfer hydrogenation of ketones has been assessed.

Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.. HPLC of Formula: C8H7NO3

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Recommanded Product: 1-(4-Nitrophenyl)ethanone. In 2020.0 NEW J CHEM published article about ANTIINFLAMMATORY ACTIVITY; PYRAZOLE DERIVATIVES; ANTIBACTERIAL; DESIGN; AGENTS; APOPTOSIS; SCAFFOLD in [Sivaramakarthikeyan, Ramar; Iniyaval, Shunmugam; Ramalingan, Chennan] Kalasalingam Acad Res & Educ Deemed Univ, Sch Adv Sci, Dept Chem, Krishnankoil 626126, Tamil Nadu, India; [Lim, Wei-Meng; Hii, Ling-Wei; Mai, Chun-Wai] Int Med Univ, Sch Pharm, 126 Jalan Jalil Perkasa 19, Kuala Lumpur 57000, Malaysia; [Mai, Chun-Wai] Int Med Univ, Inst Res Dev & Innovat IRDI, Ctr Canc & Stem Cell Res, 126 Jalan Jalil Perkasa 19, Kuala Lumpur 57000, Malaysia in 2020.0, Cited 58.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The synthesis of a series of novel pyrazolylphenanthroimidazoles 6a-6j has been accomplished utilizing a multi-step synthetic protocol, and characterized through physical and spectral techniques. Among them, the molecules possessing para-bromo (6d), para-methyl (6f) and para-nitro (6j) phenyl substituents on the pyrazole scaffold displayed similar anti-inflammatory activity and the one with no substituents on the aryl unit (6a) exhibited the highest anti-inflammatory profile. While investigating the DPPH radical scavenging activity, the synthesized chemical entity with a para-methoxyphenyl group attached at the pyrazole structural motif (6i) revealed the highest activity when compared to the other synthesized molecules. Furthermore, the evaluation of cytotoxic activity of the synthesized molecule (6a) exerted significant activity against both the pancreatic cell lines such as AsPC1 and SW1990. Besides, while performing the molecular docking studies of 6a with B-cell lymphoma 2, an appreciable binding affinity (-9.04 kcal mol(-1)) has been observed. The results of the present examination imply that these chemical entities could be used as efficient intermediates for the construction of biopertinent molecules.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Sivaramakarthikeyan, R; Iniyaval, S; Lim, WM; Hii, LW; Mai, CW; Ramalingan, C or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Quality Control of 1-(4-Nitrophenyl)ethanone. I found the field of Chemistry; Materials Science; Mineralogy very interesting. Saw the article Pd immobilized on the composite of halloysite and low-cost bio-based eutectic solvent-derived carbon: An efficient catalyst for hydrogenation in the presence of cyclodextrin published in 2020.0, Reprint Addresses Sadjadi, S (corresponding author), Iran Polymer & Petrochem Inst, Fac Petrochem, Gas Convers Dept, POB 14975-112, Tehran, Iran.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.

Using urea and glucose as cost effective and available raw materials, a eutectic solvent, was fabricated and applied as a precursor to form N-doped carbon. Subsequently, the eutectic solvent-derived carbon was reacted with halloysite nanoclay through hydrothermal process to produce a novel nanocomposite. The resultant compound was utilized as a support for the immobilization of Pd nanoparticles. The final nanocomposite was then employed as a highly active and selective catalyst for promoting hydrogenation reaction of nitroarenes in the presence of cyclodextrin as co-catalyst. To elucidate the roles of the eutectic solvent-derived carbon, halloysite and the ratio of halloysite: eutectic solvent-derived carbon in the catalysis, several control samples were prepared and their activities were compared with that of the catalyst. Furthermore, the role of cyclodextrin in the catalysis was approved by comparing the catalytic efficiency of the catalyst in the absence and the presence of cyclodextrin. It was found that cyclodextrin exerted its role via acing as phase transfer agent, while eutectic solvent-derived carbon could significantly increase the Pd loading. On the other hand, the ratio of halloysite: eutectic solvent-derived carbon could influence the performance of the catalyst. Notably, the catalyst was recyclable up to six reaction runs.

Quality Control of 1-(4-Nitrophenyl)ethanone. Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Computed Properties of C8H7NO3. Recently I am researching about ONE-POT SYNTHESIS; HIGHLY EFFICIENT; BENZYL ALCOHOLS; METHYL KETONES; BENZIMIDAZOLES; QUINAZOLINONES; BENZOXAZOLES; AMINATION; IODINE; FACILE, Saw an article supported by the IIT RoorkeeIndian Institute of Technology (IIT) – Roorkee. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Khan, D; Ahmed, N; Alsharif, MA; Alahmdi, MI; Mukhtar, S. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

An interestingcyclization reactions of aryl ketones with 2-amino aniline derivatives under SeO2 (oxidant) are described for the synthesis of benzoxazole, benzothiazole, benzimidazole and quinazolinone through the C-C cleavage of acetophenone. The reaction likely involves sequential C-N, C-O and C-S bond formation followed by C(CO)-C(alkyl) bond cleavage. Various substituted fused heterocycles are obtained in good to excellent (gram scale) yields in a single step from readily available acetophenones.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Khan, D; Ahmed, N; Alsharif, MA; Alahmdi, MI; Mukhtar, S or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem