Category: 100-19-6

Recently I am researching about PHOSPHONATE DERIVATIVES; INHIBITORS; ANTIBACTERIAL, Saw an article supported by the National Research, Development and Innovation Office (NKFIH project) [TET_16-1-2016-0111]. Published in TAYLOR & FRANCIS LTD in ABINGDON ,Authors: Kiss, NZ; Radai, Z; Keglevich, G. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone. Recommanded Product: 100-19-6

alpha-Hydroxyphosphonates have been in the focus of interest for many years due to their potential in biological activity. Not only alpha-hydroxyphosphonates are of general importance, but also their derivatives. alpha-Aminophosphonates and alpha-hydroxyphosphonic acids have already been recognized for their biological effects, while phosphoryloxyphosphonates represent a new family of compounds. In this paper we present alternative syntheses towards alpha-hydroxyphosphonates and their derivatives.

Recommanded Product: 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Kiss, NZ; Radai, Z; Keglevich, G or concate me.

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

Recently I am researching about CYCLODEXTRIN-BASED NANOSPONGES; GOLD NANOPARTICLES; NANOMATERIALS; MICROSPHERES; OXIDATION; COMPOSITE; CHEMISTRY; CLUSTERS; ENERGY; SUZUKI, Saw an article supported by the Fundamental Research Funds for the Central UniversitiesFundamental Research Funds for the Central Universities [2042016HF1054]. Quality Control of 1-(4-Nitrophenyl)ethanone. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Qi, B; Wu, CC; Liu, Y; Liu, J; Zhang, HB. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Self-assembled nanotechnology has been used widely in various well-defined microstructures fabrication. Herein, this synthetic protocol was successfully utilized to in situ or hierarchically prepare magnetic Pt nanocomposites Fe3O4@Pt via a distinguishing two-step process. The distinction of these two pathways is due to the different synthetic processes. In the case of in situ preparation (Path I), it involves a supramolecular self-assembly of boron clusters with gamma-CD on Fe3O4 substrate and then followed by in situ formation of Pt nanoparticles (NPs). But in the case of hierarchical preparation (Path II), the first step is preparing Pt NPs colloids reduced by boron clusters Cs-2[closo-B12H12], and subsequent step is immobilizing the as-prepared [closo-B12H12](2-)-capped Pt NPs on the Fe3O4@gamma-CD. The success of these two fabrication strategies lies in the use of trifunctional boron clusters (reductant, stabilizer, and superchaotropic anchor). Both of the as-prepared Fe3O4@Pt nanocomposites showed good catalytic performance in the selective nitro-group reduction of nitroaromatics. A control test further indicated that the in situ prepared Fe3O4@Pt nanocomposites, with smaller size and higher loading of Pt NPs, exhibited a better catalytic performance and recyclability.

Quality Control of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Qi, B; Wu, CC; Liu, Y; Liu, J; Zhang, HB or concate me.

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

An article Biocompatibility, in Vitro Antiproliferative, and in Silico EGFR/VEGFR2 Studies of Heteroleptic Metal(II) Complexes of Thiosemicarbazones and Naproxen WOS:000482173200010 published article about MIXED-LIGAND COMPLEXES; DNA INTERACTION; ANTICANCER ACTIVITY; ZINC(II) COMPLEXES; MOLECULAR DOCKING; GROWTH-INHIBITION; CANCER-CELLS; COPPER(II); NICKEL(II); BINDING in [Bharathi, Sundaram; Mahendiran, Dharmasivam; Rahiman, Aziz Kahlur] Univ Madras, New Coll Autonomous, Postgrad & Res Dept Chem, Chennai 600014, Tamil Nadu, India; [Mahendiran, Dharmasivam] Univ Sydney, Bosch Inst, Dept Pathol, Mol Pharmacol & Pathol Program, Sydney, NSW 2006, Australia; [Kumar, Raju Senthil] Swamy Vivekanandha Coll Pharm, Dept Pharmaceut Chem, Elayampalayam 637205, Tiruchengodu, India; [Kim, Young Guk; Gajendiran, Mani; Kim, Kyobum] Incheon Natl Univ, Sch Life Sci & Bioengn, Div Bioengn, Incheon 22012, South Korea in 2019.0, Cited 48.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Computed Properties of C8H7NO3

Eight heteroleptic nickel(II) and copper(II) complexes of the type [M(L1-4)(nap)(2)] (1-8), where L1-4 = 2-(1-(4-substitutedphenyl)ethylidene)-hydrazinecarbothioamide, nap = naproxen, and M = Ni(II) or Cu(II), have been synthesized and characterized. UV-vis and EPR spectral studies showed distorted octahedral geometry around metal(II) ions. The cyclic voltammogram of complexes 1-8 displayed an irreversible one-electron transfer process in the cathodic region (E-pc = -0.66 to -1.43 V), and nickel(II) complexes 1-4 displayed an irreversible one-electron oxidation process in the anodic region (E-pa = 0.75 to 1.10 V). The obtained magnetic moment values (1.82-1.93 mu(B)) for copper(II) complexes 5-8 indicate distortion from octahedral geometry, which is further supported by EPR studies. The geometry of the complexes is retained in both solid and solution phases as evidenced from UV-vis and EPR studies. All the complexes showed stability for almost 72 h in biologically relevant solutions. The reducing ability of the copper(II) complexes in the presence of ascorbic acid was analyzed by UV-vis and cyclic voltammetry techniques, which indicates the reduction of the copper(II) to a copper(I) center, and possible interaction within the cells. An in vitro antiproliferative study revealed the nontoxic nature of complexes to normal human dermal fibroblast (NHDF) up to a concentration of 100 ng/mL. The antiproliferative activity of the complexes was tested against three cancerous (human breast adenocarcinoma (MCF-7), hepatoma (HepG2), and lung (A549)) cell lines using MTT reduction assay, which showed enhanced activity for complexes 4 and 8 containing the hydrophobic substituent. Apoptotic and cellular uptake studies showed that complex 8 is readily taken up by HepG2 cell lines and induces ROS-mediated mitochondrial and caspase-dependent apoptosis. In silico studies indicated hydrogen bonding, hydrophobic, and pi-pair (pi-pi, pi-sigma, and pi-cation) interactions between the complexes and EGFR/VEGFR2 kinase receptors.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Bharathi, S; Mahendiran, D; Kumar, RS; Kim, YG; Gajendiran, M; Kim, K; Rahiman, AK or concate me.

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

Authors Bao, ZP; Miao, RG; Qi, XX; Wu, XF in ROYAL SOC CHEMISTRY published article about in [Bao, Zhi-Peng; Miao, Ren-Guan; Qi, Xinxin] Zhejiang Sci Tech Univ, Dept Chem, Hangzhou 310018, Zhejiang, Peoples R China; [Wu, Xiao-Feng] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Liaoning, Peoples R China; [Wu, Xiao-Feng] Inst Univ Rostock, Leibniz Inst Katalyse eV, Albert Einstein Str 29a, D-18059 Rostock, Germany in 2021, Cited 36. 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

Dimethyl carbonate (DMC), an environment-friendly compound prepared from CO2, shows diverse reactivities. In this communication, an efficient procedure using DMC as both a C1 building block and solvent in the aminocarbonylation reaction with nitro compounds has been developed. W(CO)(6) acts both a CO source and a reductant here.

Name: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Bao, ZP; Miao, RG; Qi, XX; Wu, XF or concate me.

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

Ding, YX; Ma, RC; Hider, RC; Ma, YM in [Ding, Yuxin; Ma, Renchao; Ma, Yongmin] Taizhou Univ, Sch Pharmaceut & Chem Engn, Taizhou 318000, Peoples R China; [Ding, Yuxin; Ma, Yongmin] Zhejiang Chinese Med Univ, Sch Pharmaceut Sci, Hangzhou 310053, Peoples R China; [Hider, Robert C.] Kings Coll London, Inst Pharmaceut Sci, Franklin Wilkins Bldg,Stamford St, London SE1 9NH, England published Acid-Catalyzed Pseudo Five-Component Annulation for a General One-Pot Synthesis of 2,4,6-Triaryl Pyrimidines in 2020.0, Cited 65.0. SDS of cas: 100-19-6. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A facile and general synthesis of 2,4,6-triaryl pyrimidines has been developed. It involves a one-pot [2+1+1+1+1] pseudo five-component annulation of one methyl ketone, two aldehydes and two NH4OAc catalyzed by TfOH. One C-C and four C-N bonds are formed during the oxidative annulation process. The reaction shows good tolerance of many important functional groups in air and produces only water as the coproduct, making this methodology a highly versatile alternative to the existing methods for structuring pyrimidine framework.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Ding, YX; Ma, RC; Hider, RC; Ma, YM or concate me.. SDS of cas: 100-19-6

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

I found the field of Chemistry very interesting. Saw the article Transfer Hydrogenation of Ketones and Imines with Methanol under Base-Free Conditions Catalyzed by an Anionic Metal-Ligand Bifunctional Iridium Catalyst published in 2020.0. Product Details of 100-19-6, Reprint Addresses Li, F (corresponding author), Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

An anionic iridium complex [Cp*Ir(2,2′-bpyO)(OH)][Na] was found to be a general and highly efficient catalyst for transfer hydrogenation of ketones and imines with methanol under base-free conditions. Readily reducible or labile substituents, such as nitro, cyano, and ester groups, were tolerated under present reaction conditions. Notably, this study exhibits the unique potential of anionic metal-ligand bifunctional iridium catalysts for transfer hydrogenation with methanol as a hydrogen source.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Wang, RZ; Han, XY; Xu, J; Liu, P; Li, F or concate me.. Product Details of 100-19-6

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

An article Nitrate promoted mild and versatile Pd-catalysed C(sp(2))-H oxidation with carboxylic acids WOS:000565016900018 published article about C-H; DIRECT ACYLOXYLATION; BENZOXYLATION; BONDS; ACTIVATION; ARYL; NOX in [Xiong, Xue; Mao, Yang-Jie; Hao, Hong-Yan; He, Yu-Ting; Xu, Zhen-Yuan; Lou, Shao-Jie; Xu, Dan-Qian] Zhejiang Univ Technol, Coll Chem Engn, Key Lab Green Pesticides & Cleaner Prod Technol Z, Catalyt Hydrogenat Res Ctr,State Key Lab Breeding, Hangzhou 310014, Peoples R China; [Luo, Gen] Anhui Univ, Inst Phys Sci & Informat Technol, Hefei 230601, Peoples R China in 2020, Cited 30. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. COA of Formula: C8H7NO3

A nitrate-promoted Pd-catalysed mild cross-dehydrogenative C(sp(2))-H bond oxidation of oximes or azobenzenes with diverse carboxylic acids has been developed. In contrast to the previous catalytic systems, this protocol features mild conditions (close to room temperature for most cases) and a broad substrate scope (up to 64 examples), thus constituting a versatile method to directly prepare diverseO-aryl esters. Moreover, the superiority of the nitrate additive in this mild transformation was further determined by experimental and computational evidence.

COA of Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Xiong, X; Mao, YJ; Hao, HY; He, YT; Xu, ZY; Luo, G; Lou, SJ; Xu, DQ or concate me.

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

Authors Gaikwad, R; Bobde, Y; Ganesh, R; Patel, T; Rathore, A; Ghosh, B; Das, K; Gayen, S in TAYLOR & FRANCIS INC published article about INDOLE MOLECULES; INHIBITORS; DESIGN; INDOLE-3-CARBINOL; SCAFFOLD; ANALOGS; NEDD4-1; POTENT in [Gaikwad, Ruchi; Patel, Tarun; Rathore, Anju; Gayen, Shovanlal] Dr Hari Singh Gour Vishwavidyalaya, Dept Pharmaceut Sci, Lab Drug Design & Discovery, Sagar 470003, Madhya Pradesh, India; [Bobde, Yamini; Ganesh, Routholla; Ghosh, Balaram] BITS Pilani, Dept Pharm, Hyderabad Campus, Hyderabad, India; [Das, Kalpataru] Dr Hari Singh Gour Vishwavidyalaya, Dept Chem, Adv Organ Synth Lab, Sagar 470003, Madhya Pradesh, India in 2019.0, Cited 38.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Indole derivatives have attractive anticancer properties and may be a future hope for better anticancer drug(s) of low toxicity and high potency. In this paper, syntheses of 2-phenylindole derivatives have been described via Fischer indole synthesis through a one-pot solvent-free method. The synthesized compounds were screened for anticancer potential in vitro against murine melanoma (B16F10), human lung cancer (A549), and human breast cancer (MDA-MB-231) cell lines. The results highlighted that 2-phenylindole derivatives are also promising anticancer agents in case of melanoma and lung cancer along with the breast cancer. Molecular docking analyses with possible targets for melanoma (NEDD4-1) and lung cancer (EGFR) were also performed to understand specific interactions of 2-phenylindole derivatives with the amino acid residues of the receptors.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Gaikwad, R; Bobde, Y; Ganesh, R; Patel, T; Rathore, A; Ghosh, B; Das, K; Gayen, S or concate me.. Category: benzodioxans

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

Computed Properties of C8H7NO3. Recently I am researching about MOLECULAR DOCKING; ELLIPTICINE DERIVATIVES; ANTIFUNGAL ACTIVITY; AMIDE DERIVATIVES; POTENT; FLAVONOIDS; INHIBITORS; DISCOVERY; ANALOGS; CLK1, Saw an article supported by the . Published in SPRINGER BIRKHAUSER in NEW YORK ,Authors: Suma, VR; Sreenivasulu, R; Rao, MVB; Subramanyam, M; Ahsan, MJ; Alluri, R; Rao, KRM. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

A novel library of chalcone linked thiazole-imidazopyridine (12a-j) derivatives were designed, synthesized, and their structures were characterized by(1)H NMR,C-13 NMR and mass spectral studies. Further, all compounds were tested for their anticancer effects on four human cancer cell lines including MCF-7 (breast carcinoma), A549 (lung carcinoma), DU-145 (prostate carcinoma) and MDA MB-231 (breast carcinoma) by employing MTT method, using etoposide as the positive control. Among them, compound12bdisplayed more potent anticancer activity against four cancer cell lines when compared to the positive control.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Suma, VR; Sreenivasulu, R; Rao, MVB; Subramanyam, M; Ahsan, MJ; Alluri, R; Rao, KRM or concate me.. Computed Properties of C8H7NO3

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

An article Highly efficient and practical aerobic oxidation of alcohols by inorganic-ligand supported copper catalysis WOS:000484021100008 published article about MOLECULAR-OXYGEN; SELECTIVE OXIDATION; BENZYLIC ALCOHOLS; BUILDING-BLOCKS; METAL-CATALYSTS; ALDEHYDES; MILD; POLYOXOMETALATE; KETONES; GREEN in [Wei, Zheyu; Ru, Shi; Zhao, Qixin; Yu, Han] Shanghai Inst Technol, Sch Chem & Environm Engn, 100 Haiquan Rd, Shanghai 201418, Peoples R China; [Yu, Han; Wei, Yongge] Tsinghua Univ, Dept Chem, Key Lab Organ Optoelect & Mol Engn, Minist Educ, Beijing 100084, Peoples R China; [Zhang, Gang] Sichuan Univ, Inst Mat Sci & Technol, Chengdu 610064, Sichuan, Peoples R China; [Zhang, Gang] Sichuan Univ, Analyt & Testing Ctr, Chengdu 610064, Sichuan, Peoples R China in 2019.0, Cited 66.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

The oxidation of alcohols to aldehydes or ketones is a highly relevant conversion for the pharmaceutical and fine-chemical industries, and for biomass conversion, and is commonly performed using stoichiometric amounts of highly hazardous oxidants. The aerobic oxidation of alcohols with transition metal complex catalysts previously required complicated organic ligands and/or nitroxyl radicals as co-catalysts. Herein, we report an efficient and eco-friendly method to promote the aerobic oxidation of alcohols using an inorganic-ligand supported copper catalyst 1, (NH4)(4)[CuMo6O18(OH)(6)], with O-2 (1 atm) as the sole oxidant. Catalyst 1 is synthesized directly from cheap and commonly available (NH4)(6)Mo7O24 center dot 4H(2)O and CuSO4, which consists of a pure inorganic framework built from a central Cu-II core supported by six (MoO6)-O-VI inorganic scaffolds. The copper catalyst 1 exhibits excellent selectivity and activity towards a wide range of substrates in the catalytic oxidation of alcohols, and can avoid the use of toxic oxidants, nitroxyl radicals, and potentially air/moisture sensitive and complicated organic ligands that are not commercially available. Owing to its robust inorganic framework, catalyst 1 shows good stability and reusability, and the catalytic oxidation of alcohols with catalyst 1 could be readily scaled up to gram scale with little loss of catalytic activity, demonstrating great potential of the inorganic-ligand supported Cu catalysts in catalytic chemical transformations.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Wei, ZY; Ru, S; Zhao, QX; Yu, H; Zhang, G; Wei, YG or concate me.. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

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