Month: October 2021

An article Synthesis of pi-Extended Imidazoles by 1,3-Dipolar Cycloaddition of Polycyclic Aromatic Azomethine Ylides with Nitriles WOS:000562077400082 published article about FLUOROCARBON DERIVATIVES; NITROGEN; SILVER; ACID; CONSTRUCTION; COORDINATION; HYDROCARBONS; INDOLIZINES in [Li, Qiang-Qiang; Ochiai, Kotaro; Lee, Cherie-Anne; Ito, Shingo] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 637371, Singapore in 2020, Cited 68. Formula: C14H11N. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3

Here we report the 1,3-dipolar cycloaddition of polycyclic aromatic azomethine ylides with nitriles to produce highly fused imidazole derivatives, that is, tribenzo[b,g,ij]imidazo-[2,1,5-de]quinolizine. The advantages of this transformation are the broad substrate scope and the good functional group compatibility. The subsequent palladium-catalyzed intramolecular cyclization provides an efficient approach to further pi-extended imidazoles, that is, 14b(1),15-diazadibenzo[fg,ij]cyclopenta[rst]pentaphene.

About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Li, QQ; Ochiai, K; Lee, CA; Ito, S or concate me.. Formula: C14H11N

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

I found the field of Chemistry very interesting. Saw the article Effect of Confined Spaces in the Catalytic Activity of 1D and 2D Heterogeneous Carbon-Based Catalysts for Synthesis of 1,3,5-Triarylbenzenes: RGO-SO3H vs. MWCNTs-SO3H published in 2019.0. Name: 1-(4-Nitrophenyl)ethanone, Reprint Addresses Golestanzadeh, M; Naeimi, H (corresponding author), Univ Kashan, Dept Organ Chem, Fac Chem, Kashan 8731781167, Iran.; Golestanzadeh, M (corresponding author), Isfahan Univ Med Sci, Res Inst Primordial Prevent Non Communicable Dis, Environm Res Ctr, Esfahan 8174673461, Iran.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

One hot debate between catalytic activities of sulfonated reduced graphene oxide (RGO-SO3H), as the 2D heterogeneous carbon-based catalyst, and sulfonated multi-walled carbon nanotubes (MWCNTs-SO3H), as the 1D heterogeneous carbon-based catalyst, was investigated in the synthesis of 1,3,5-triarylbenzenes under different conditions. This comparison study revealed that the 2D catalytic system was more efficient relative to the 1D catalyst in terms of yields of the target products, turnover frequency of the catalyst (TOF), and the reusability. The reasons of this observation such as specific surface area, confinement spaces in 1D and 2D carbon-based catalysts, solvent accessible surface area, surface active sites, and the availability of supported functional groups on carbon nanostructures will discuss. Moreover, the application of synthesized compounds as a substrate was checked in carbon-carbon bond formation. Also, one of the synthesized compounds was produced using three approaches under metal and non-metal conditions. Notably, the recyclability of the two catalytic systems was checked.

Name: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Golestanzadeh, M; Naeimi, H or concate me.

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

An article Hybrids of Isatin-Pyrazole as Potential alpha-Glucosidase Inhibitors: Synthesis, Biological Evaluations and Molecular Docking Studies WOS:000514098900024 published article about IN-VITRO EVALUATION; DISCOVERY; DERIVATIVES; MANAGEMENT; AGENTS in [Kaur, Ramandeep; Palta, Kezia; Kumar, Manoj] Panjab Univ, Univ Inst Pharmaceut Sci, Chandigarh 160014, India in 2019.0, Cited 34.0. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

alpha-Glucosidase inhibition has been considered as an effective strategy for controlling the post-prandial hyperglycemia in diabetic patients. A series of novel isatin-pyrazole hybrids has been rationally designed, synthesized and characterized by different spectroscopic techniques. All of the synthesized compounds were evaluated for their alpha-glucosidase inhibitory potential using in vitro enzymatic assay. The tested compounds have exhibited potent alpha-glucosidase inhibition with IC50 values ranging from 3.26 +/- 0.25 to 32.33 +/- 1.08 mu M. Compound V7, having 3-nitro phenyl ring appended at pyrazole nucleus, has emerged as the most potent inhibitor among the series with an IC50 value of 3.26 +/- 0.25 mu M, which was approximately 146 fold more potent than the clinically used drug acarbose (IC50 = 478.07 +/- 1.53 mu M). Molecular docking studies were carried out to investigate the binding interactions of most active compounds with the active site of the enzyme. Further, in silico predictive pharmacokinetic parameters (ADME) and drug-like properties of the compounds were within the acceptable ranges. In vivo biological evaluations further supplemented the in vitro results.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Kaur, R; Palta, K; Kumar, M or concate me.. Formula: C8H7NO3

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

Brondani, PB; Mittersteiner, M; Voigt, MA; Klinkowski, BH; Scharf, DR; de Jesus, PC in [Brondani, Patricia Bulegon; Voigt, Morgana Aline] Univ Fed Santa Catarina, Dept Ciencias Exatas & Educ, BR-89036256 Blumenau, SC, Brazil; [Mittersteiner, Mateus; Klinkowski, Bruna Heloisa; Scharf, Dilamara Riva; de Jesus, Paulo Cesar] Univ Reg Blumenau, Dept Quim, BR-89019917 Blumenau, SC, Brazil published Synthetic Versatility of Lipases: Application for Si-O Bond Formation and Cleavage in 2019.0, Cited 35.0. Computed Properties of C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Several commercially available lipases were examined in a study on O-Si bond formation and cleavage applying silicon-based protecting groups and alcohols or the corresponding silyl ethers. With regard to deprotection, from silyl ether to the corresponding alcohol, only the solvent and the lipase were necessary. The influence of the protecting group, the lipase source, and the substituent was investigated to optimize the results. The TMS moiety could be removed in 24 hours of reaction at room temperature in aqueous systems (conv. up to 99%, depending on the substrate and lipase). The reverse reactions, that is, with the protection of the alcohols, were carried out in hexane using different silyl chlorides. The TMS, TES, and TBS moieties were successfully inserted in the primary and secondary alcohols without the need for dry conditions or an inert atmosphere, presenting conversions of up to 99%, depending on the substrate.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Brondani, PB; Mittersteiner, M; Voigt, MA; Klinkowski, BH; Scharf, DR; de Jesus, PC or concate me.

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

Safety of 1-(4-Nitrophenyl)ethanone. In 2021.0 J ORG CHEM published article about CARBENE INSERTION; CONSTRUCTION; INHIBITORS; ACCESS in [Wu, Ye-bin; Wu, You-zhi; Wu, Jian; Xu, Dan; Ma, Chang-you] Nanjing Chia Tai Tianqing Pharmaceut Co Ltd, Qixia Nanjing 210046, Jiangsu, Peoples R China; [Jiang, Hui; Chang, Wen-wu] Pharmaron Shang Hai, Shanghai 201203, Peoples R China in 2021.0, Cited 34.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The highly regioselective N-alkylation reaction of 2-pyridones was achieved through hydrazone chemistry, especially for substrates with bulky secondary alkyl groups. Described herein is a copper-catalyzed coupling reaction of pyridone derivatives with tosylhydrazones.

Safety of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Wu, YB; Wu, YZ; Wu, J; Xu, D; Jiang, H; Chang, WW; Ma, CY or concate me.

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

I found the field of Chemistry very interesting. Saw the article Hydration of terminal alkynes catalyzed by cobalt corrole complex published in 2020.0. Quality Control of 1-(4-Nitrophenyl)ethanone, Reprint Addresses Liu, HY (corresponding author), South China Univ Technol, Dept Chem, Key Lab Funct Mol Engn Guangdong Prov, Guangzhou 510640, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Cobalt(III) corrole was firstly applied to the hydration of terminal alkynes. The alkyne hydration proceeded in good to excellent yield with 0.03 to 0.3 mol% cobalt corrole catalyst loading. A wide range of substrates were tolerated. Particularly, the reaction can give 90% yield in a gram scale experiment. (C) 2020 Elsevier Ltd. All rights reserved.

Quality Control of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Lai, JW; Liu, ZY; Chen, XY; Zhang, H; Liu, HY or concate me.

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

An article Microwave-Assisted Synthesis as an Efficient Method to Enhance the Catalytic Activity of Zr-Based Metal Organic Framework UiO-66 in a Heterocyclization Reaction WOS:000500019700001 published article about DEFECTS; QUINAZOLINONES; OPTIMIZATION; MOF in [Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thi Dang, Y.; Tan Le Hoang Doan] Vietnam Natl Univ Ho Chi Minh City VNU HCM, Ctr Innovat Mat & Architectures INOMAR, Ho Chi Minh City 721337, Vietnam; [Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Phuong Hoang Tran; Tan Le Hoang Doan] Vietnam Natl Univ Ho Chi Minh City, Dept Organ Chem, Fac Chem, Univ Sci, Ho Chi Minh City 721337, Vietnam in 2019.0, Cited 50.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Quality Control of 1-(4-Nitrophenyl)ethanone

Zr-based metal-organic frameworks have been considered promising heterogeneous catalysts in various reactions. It has been proven that the defect sites in these frameworks, which result from deficiency of linkers, could act as the reaction active sites. In this work, microwave irradiation was used for rapid synthesis and increasing defects on Zr-6 clusters of metal-organic framework UiO-66. Powder X-ray diffraction, thermal gravimetric analysis, and N-2 sorption isotherms were performed to characterize and calculate the defect number in the framework. UiO-66 prepared by microwave method for a few minutes could reach 1.8 missing linkers per cluster. The material with acetic acid as a co-catalyst showed highly heterogeneous catalytic activity in the solvent-free heterocyclization of 2,2-disubstituted 2,3-dihydroquinazolin-4(1H)-ones from anthranilamide and ketones/aldehydes. The synthetic scheme consisted of zirconium cluster catalysed carbonyl group of anthranilamide to achieve the C-N propitious combination and succeeding ring closure process.

Quality Control of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Nguyen, LHT; Nguyen, TTT; Dang, YT; Tran, PH; Doan, TLH or concate me.

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

I found the field of Chemistry very interesting. Saw the article Cu-Catalyzed Diastereo- and Enantioselective Reactions of gamma,gamma-Disubstituted Allyldiboron Compounds with Ketones published in 2020.0. Product Details of 100-19-6, Reprint Addresses Meek, SJ (corresponding author), Univ North Carolina Chapel Hill, Dept Chem, Chapel Hill, NC 27599 USA.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

A catalytic diastereo- and enantioselective method for the preparation of complex tertiary homoallylic alcohols containing a vicinal quaternary carbon stereogenic center and a versatile alkenylboronic ester is disclosed. Transformations are promoted by 5 mol % of a readily available copper catalyst bearing a bulky monodentate phosphoramidite ligand, which is essential for attaining both high dr and er. Reactions proceed with a wide variety of ketones and allylic 1,1-diboronate reagents, which enables the efficient preparation of diverse array of molecular scaffolds.

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zanghi, JM; Meek, SJ or concate me.

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

HPLC of Formula: C8H7NO3. I found the field of Chemistry very interesting. Saw the article Porous FeO(OH) Dispersed on Mg-Al Hydrotalcite Surface for One-Pot Synthesis of Quinoline Derivatives published in 2021.0, Reprint Addresses Motokura, K (corresponding author), Tokyo Inst Technol, Sch Mat & Chem Technol, Dept Chem Sci & Engn, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268502, Japan.; Motokura, K (corresponding author), Japan Sci & Technol Agcy JST, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan.; Motokura, K (corresponding author), Yokohama Natl Univ, Dept Chem & Life Sci, Hodogaya Ku, 79-5 Tokiwadai, Yokohama, Kanagawa 2408501, Japan.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.

The use of ubiquities elements such as iron instead of expensive precious metals as catalysts is one goal toward realizing environmentally benign synthetic chemistry. Here, we report that porous FeO(OH) dispersed on Mg-Al hydrotalcite acts as a bifunctional heterogeneous catalyst in the one-pot synthesis of 2-substituted quinoline derivatives through dehydrogenative oxidation-cyclization reactions. The catalyst was prepared by a simple grafting method using FeCl3 and Mg-Al hydrotalcite. The prepared porous FeO(OH) possesses a higher surface area than those previously reported for alpha-FeO(OH) particles. The one-pot quinoline synthesis proceeded effectively under non-noble-metal catalysis in air without requiring additional homogeneous bases or solvents.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Motokura, K; Ozawa, N; Sato, R; Manaka, Y; Chun, WJ or concate me.. HPLC of Formula: C8H7NO3

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

Quality Control of 1-(4-Nitrophenyl)ethanone. In 2021.0 EUR J MED CHEM published article about BIOLOGICAL EVALUATION; DERIVATIVES; ANALOGS in [Huo, Xian-Sen; Jian, Xie-Er; Ou-Yang, Jie; Chen, Lin; Yang, Fang; Lv, Dong-Xin; You, Wen-Wei; Rao, Jin-Jun; Zhao, Pei-Liang] Southern Med Univ, Sch Pharmaceut Sci, Guangdong Prov Key Lab New Drug Screening, Guangzhou 510515, Peoples R China in 2021.0, Cited 10.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Y By removing 5-methyl and 6-acetyl groups in our previously reported compound 3, we designed a series of novel 2,7-diaryl-[1,2,4]triazolo[1,5-a]pyrimidine derivatives as potential tubulin polymerization inhibitors. Among them, compound 5e displayed low nanomolar antiproliferative efficacy on HeLa cells which was 166-fold higher than the lead analogue 3. Interestingly, 5e displayed significant selectivity in inhibiting cancer cells over HEK-293 (normal human embryonic kidney cells). In addition, 5e dose-dependently arrested HeLa in G2/M phase through the alterations of the expression levels of p-cdc2 and cyclin B1, and caused HeLa cells apoptosis by regulation of expressions of cleaved PARP. Further evidence demonstrated that 5e effectively inhibited tubulin polymerization and was 3-fold more powerful than positive control CA-4. Moreover, molecular docking analysis indicated that 5e overlapped well with CA-4 in the colchicine-binding site. These studies demonstrated that 2,7-diaryl-[1,2,4]triazolo [1,5-a]pyrimidine skeleton might be used as the leading unit to develop novel tubulin polymerization inhibitors as potential anticancer agents. (C) 2021 Elsevier Masson SAS. All rights reserved.

Quality Control of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Huo, XS; Jian, XE; Ou-Yang, J; Chen, L; Yang, F; Lv, DX; You, WW; Rao, JJ; Zhao, PL or concate me.

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