Month: October 2021

Akasapu, K; Ojah, N; Gupta, AK; Choudhury, AJ; Mishra, P in [Akasapu, Kumudhini; Gupta, Arun Kumar; Mishra, Poonam] Tezpur Univ, Dept Food Engn & Technol, Tezpur 784028, Assam, India; [Ojah, Namita; Choudhury, Arup Jyoti] Tezpur Univ, Dept Phys, Tezpur 784028, Assam, India published An innovative approach for iron fortification of rice using cold plasma in 2020, Cited 24. HPLC of Formula: C14H11N. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3.

In the present study, an innovative cold plasma treatment was used as a tool to fortify the white rice. The amounts of ferrous sulphate and ascorbic acid were optimized for improving the bioavailability of iron. White rice samples were treated with plasma at a constant voltage of 20 kV for varying time (10 min and 15 min). The exposure time of plasma was selected based on the surface characteristics, hydrophilicity and thermal properties. Significant improvement was observed in the characteristics of hydrophilicity, surface energy, cooking time and hardness of plasma-treated rice. Plasma treated rice was fortified with the optimum concentrations of iron and ascorbic acid solution. Optimum concentrations of iron and ascorbic acid per 100 g of rice (862.93 mg and 1398.27 mg) were found by conducing experiments using Central Composite Design of Response Surface Methodology. Further, rice was blended with untreated rice in the ratio of 1:100 and 1:200 and was packed in LDPE and PP pouches and was stored at ambient temperature for further storage analysis. The in vitro bioavailability of iron was significantly higher in the plasma-treated fortified rice at both 1.35 and 7.5 pH than in the control sample, and plasma treatment significantly reduced the rate of oxidation of iron during storage.

HPLC of Formula: C14H11N. About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Akasapu, K; Ojah, N; Gupta, AK; Choudhury, AJ; Mishra, P or concate me.

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

Recently I am researching about HIGHLY ENANTIOSELECTIVE SYNTHESIS; REDUCTIVE AMINATION; F-BINAPHANE; EFFICIENT; COMPLEXES; KETONES, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21272271, 21472240]; Fourth Military Medical University [2018XA009]. Name: 1-(4-Nitrophenyl)ethanone. Published in ELSEVIER in AMSTERDAM ,Authors: Zhang, DX; Zhou, XW; Liu, RX; Li, MQ; Li, XY; Jiang, R; Nie, HF; Zhang, SY. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The Ir-catalyzed asymmetric hydrogenation of acyclic aromatic N-aryl imines with Josiphos-type binaphane ligands has been described. Under the optimized conditions, a wide range of imines were hydrogenated to afford the corresponding chiral amines in high yields (up to 94%) and good to excellent enantioselectivities (up to > 99% ee). The synthetic utility of the present protocol has been demonstrated through the asymmetric synthesis of the key chiral intermediates of calcium sensing receptor modulators on a gram scale.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zhang, DX; Zhou, XW; Liu, RX; Li, MQ; Li, XY; Jiang, R; Nie, HF; Zhang, SY or concate me.. Quality Control of 1-(4-Nitrophenyl)ethanone

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

I found the field of Biochemistry & Molecular Biology; Chemistry very interesting. Saw the article Synthesis, Structure and In Vitro Anti-Trypanosomal Activity of Non-Toxic Arylpyrrole-Based Chalcone Derivatives published in 2020.0. Recommanded Product: 100-19-6, Reprint Addresses Khanye, SD (corresponding author), Rhodes Univ, Fac Sci, Dept Chem, ZA-6140 Grahamstown, South Africa.; Khanye, SD (corresponding author), Rhodes Univ, Ctr Chem & Biomed Res, ZA-6140 Grahamstown, South Africa.; Khanye, SD (corresponding author), Rhodes Univ, Fac Pharm, Div Pharmaceut Chem, ZA-6140 Grahamstown, South Africa.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

With an intention of identifying chalcone derivatives exhibiting anti-protozoal activity, a cohort of relatively unexplored arylpyrrole-based chalcone derivatives were synthesized in moderate to good yields. The resultant compounds were evaluated in vitro for their potential activity against a cultured Trypanosoma brucei brucei 427 strain. Several compounds displayed mostly modest in vitro anti-trypanosomal activity with compounds 10e and 10h emerging as active candidates with IC50 values of 4.09 and 5.11 mu M, respectively. More importantly, a concomitant assessment of their activity against a human cervix adenocarcinoma (HeLa) cell line revealed that these compounds are non-toxic.

Recommanded Product: 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zulu, AI; Oderinlo, OO; Kruger, C; Isaacs, M; Hoppe, HC; Smith, VJ; Veale, CGL; Khanye, SD or concate me.

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

Authors Williams, UJ in AMER CHEMICAL SOC published article about in [Williams, Ursula J.] Juniata Coll, Dept Chem & Biochem, Huntingdon, PA 16652 USA in 2020.0, Cited 13.0. Quality Control 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

The Organisation for the Prohibition of Chemical Weapons (OPCW) has identified education and outreach as vital to global efforts that emphasize the responsible use of chemicals. To promote students’ exposure to broad-reaching applications of analytical chemistry, a chemical-weapons-themed project was implemented in an upper-level analytical chemistry course. In this project, students developed laboratory and data analysis skills needed to complete organic structure analysis, professionally communicated their data and conclusions, and considered chemical analysis in an applied context. This project grounds the topic of multiuse chemicals in a case-based, active-learning context.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Williams, UJ or concate me.. COA of Formula: C8H7NO3

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

Safety of 1-(4-Nitrophenyl)ethanone. I found the field of Chemistry very interesting. Saw the article Organocatalytic asymmetric vinylogous 1,4-addition of alpha,alpha-Dicyanoolefins to chalcones under a bio-based reaction media: Discovery of new Michael adducts with antiplasmodial activity published in 2019.0, Reprint Addresses Correa, AG (corresponding author), Univ Fed Sao Carlos, Ctr Excellence Res Sustainable Chem, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.

The organocatalysed asymmetric vinylogous Michael addition of alpha,alpha-dicyanoolefins to alpha,beta-unsaturated aldehydes and ketones have been reported in the last decade, however, chalcones have been poorly explored. Moreover, a considerable part of the publications in this theme still employs undesirable solvents, such as toluene and THF, with concerns related to health and environmental safety. We report herein the use of a bifunctional catalyst derived from a Cinchona alkaloid to perform the enantio- and diastereoselective Michael addition of alpha,alpha-dicyanoolefins to chalcones using 2-MeTHF as solvent. The Michael adducts were obtained in moderate to good yields and were evaluated for their antiplasmodial and cytotoxic activity. (C) 2019 Elsevier Ltd. All rights reserved.

Safety of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Martelli, LSR; Vieira, LCC; Paixao, MW; Zukerman-Schpector, J; de Souza, JO; Aguiar, ACC; Oliva, G; Guido, RVC; Correa, AG or concate me.

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

Recently I am researching about REDUCTIVE DECYANATION; CATALYZED CYANATION; LITHIUM REAGENTS; METAL EXCHANGE; CHEMISTRY ARC; POTASSIUM; GRIGNARD; HYDROCYANATION; DERIVATIVES; ALKYLATIONS, Saw an article supported by the NSERCNatural Sciences and Engineering Research Council of Canada (NSERC); Canada Foundation for InnovationCanada Foundation for InnovationCGIAR [35261]; Ontario Research Fund; University of TorontoUniversity of Toronto. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Alazet, S; West, MS; Patel, P; Rousseaux, SAL. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile. HPLC of Formula: C14H11N

The efficient preparation of nitrile-containing building blocks is of interest due to their utility as synthetic intermediates and their prevalence in pharmaceuticals. As a result, significant efforts have been made to develop methods to access these motifs which rely on safer and non-toxic sources of CN. Herein, we report that 2-methyl-2-phenylpropanenitrile is an efficient, non-toxic, electrophilic CN source for the synthesis of nitrile-bearing quaternary centers by a thermodynamic transnitrilation and anion-relay strategy. This one-pot process leads to nitrile products resulting from the gem-difunctionalization of alkyl lithium reagents.

HPLC of Formula: C14H11N. Welcome to talk about 86-29-3, If you have any questions, you can contact Alazet, S; West, MS; Patel, P; Rousseaux, SAL or send Email.

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

In 2020.0 CHINESE J STRUC CHEM published article about HOMOGENEOUS CATALYSIS; HETEROGENEOUS CATALYSTS; HYDROGENATION; PD; REDUCTION; NANOPARTICLES; NITROARENES; RECOVERY; LAYER; MONODISPERSE in [Chen Yan-Ning; Li Jing-Jun; Yang Wei-Guang] Fuzhou Univ, Coll Chem, Fuzhou 350002, Peoples R China; [Chen Yan-Ning; Li Jing-Jun; Yang Wei-Guang; Gao Shui-Ying] Chinese Acad Sci, Fujian Inst Res Struct Matter, State Key Lab Struct Chem, Fuzhou 350002, Peoples R China in 2020.0, Cited 34.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 1-(4-Nitrophenyl)ethanone

This work presents a highly active and reusable heterogeneous film catalytic assembly for hydrogenation reduction of aromatic nitro compounds. The multilayer structures of PEI-(K2PdCl4-P1)(n)-film (PEI = polyethylenmine, P1 = 3-amino-3-(4-pyridinyl)-propionitrile) bound to quartz slides were fabricated by layer-by-layer (LbL) self-assembly method. Various characterization techniques including X-ray photoelectron spectroscopy (XPS), inductively coupled plasma OES spectrometer (ICP), UV-vis spectroscopy and atomic force microscopy (AFM) were employed to reveal the growth process of the resulting LbL multilayers in detail. Subsequent in situ reduction by H-2 produced Pd nanoparticles embedded in such films were used as catalyst for the hydrogenation of nitroarenes. The catalytic performance test shows that the thin film catalyst can be applied to the hydrogenation reaction of various substituted nitroaromatics, and exhibits good catalytic activity and good catalyst stability. It is worth mentioning that our catalytic films can be easily removed from the reaction system in any time during the reaction, and the catalytic activity could be fully recovered when reused directly in another catalytic cycle for five times.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Chen, YN; Li, JJ; Yang, WG; Gao, SY or send Email.

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

Authors Li, PG; Zhu, H; Fan, M; Yan, C; Shi, K; Chi, XW; Zou, LH in ROYAL SOC CHEMISTRY published article about DOUBLE CARBONYLATION; TERMINAL ALKYNES; C-H; ENANTIOSELECTIVE SYNTHESIS; OXIDATIVE AMIDATION; OXOCARBOXYLIC ACIDS; CHLOROPEPTIN-I; FKBP12 LIGANDS; ARYL IODIDES; DERIVATIVES in [Li, Ping-Gui; Zhu, Hao; Fan, Min; Yan, Cheng; Shi, Kai; Chi, Xi-Wen; Zou, Liang-Hua] Jiangnan Univ, Minist Educ, Sch Pharmaceut Sci, Key Lab Carbohydrate Chem & Biotechnol, Lihu Ave 1800, Wuxi 214122, Jiangsu, Peoples R China; [Li, Ping-Gui] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Xianlin Ave 163, Nanjing 210093, Jiangsu, Peoples R China in 2019.0, Cited 76.0. Recommanded Product: 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Copper-catalyzed coupling of alpha-keto acids with anthranils is reported for the synthesis of alpha-ketoamides. This process involves N-O/C-O bond cleavages and C-N bond formation. Furthermore, the decarboxylation of alpha-keto acids can be successfully suppressed under redox-neutral conditions.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Li, PG; Zhu, H; Fan, M; Yan, C; Shi, K; Chi, XW; Zou, LH or send Email.

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

I found the field of Biochemistry & Molecular Biology; Chemistry very interesting. Saw the article Mono- or di-substituted imidazole derivatives for inhibition of acetylcholine and butyrylcholine esterases published in 2019.0. SDS of cas: 100-19-6, Reprint Addresses Menges, N (corresponding author), Van Yuzuncu Yil Univ, Pharmaceut Chem Sect, TR-65080 Van, Turkey.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Mono- or di-substituted imidazole derivatives were synthesized using a one-pot, two-step strategy. All imidazole derivatives were tested for AChE and BChE inhibition and showed nanomolar activity similar to that of the test compound donepezil and higher than that of tacrine. Structure activity relationship studies, docking studies to on X-ray crystal structure of AChE with PDB code 1B41, and adsorption, distribution, metabolism, and excretion (ADME) predictions were performed. The synthesized core skeleton was bound to important regions of the active site of AChE such as the peripheral anionic site (PAS), oxyanion hole (OH), and anionic subsite (AS). Selectivity of the reported test compounds was calculated and enzyme kinetic studies revealed that they behave as competitive inhibitors, while two of the test compounds showed noncompetitive inhibitory behavior. ADME predictions revealed that the synthesized molecules might pass through the blood brain barrier and intestinal epithelial barrier and circulate freely in the blood stream without binding to human serum albumin. While the toxicity of one compound on the WS1 (skin fibroblast) cell line was 1790 mu M, its toxicity on the SH-SY5Y (neuroblastoma) cell line was 950 mu M.

SDS of cas: 100-19-6. Welcome to talk about 100-19-6, If you have any questions, you can contact Kuzu, B; Tan, M; Taslimi, P; Gulcin, I; Taspinar, M; Menges, N or send Email.

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

Name: 1-(4-Nitrophenyl)ethanone. In 2020.0 POLYMERS-BASEL published article about ARAMIDS AROMATIC POLYAMIDES; POLYMERS; ACID in [Trigo-Lopez, Miriam; Sanjuan, Ana M.; Mendia, Aranzazu; Munoz, Asuncion; Garcia, Felix C.; Garcia, Jose M.] Univ Burgos, Fac Ciencias, Dept Quim, Plaza Misael Banuelos S-N, Burgos 09001, Spain in 2020.0, Cited 38.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

We prepared high-performance aromatic copolyamides, containing bithiazole and thiazolo-thiazole groups in their main chain, from aromatic diamines and isophthaloyl chloride, to further improve the prominent thermal behavior and exceptional mechanical properties of commercial aramid fibers. The introduction of these groups leads to aramids with improved strength and moduli compared to commercialmeta-oriented aromatic polyamides, together with an increase of their thermal performance. Moreover, their solubility, water uptake, and optical properties were evaluated in this work.

Name: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Trigo-Lopez, M; Sanjuan, AM; Mendia, A; Munoz, A; Garcia, FC; Garcia, JM or send Email.

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