Month: October 2021

Category: benzodioxans. Carpentier, F; Felpin, FX; Zammattio, F; Le Grognec, E in [Carpentier, Florian; Felpin, Francois-Xavier; Zammattio, Francoise; Le Grognec, Erwan] Univ Nantes, CNRS, CEISAM, UMR 6230, F-44000 Nantes, France published Synthesis of 5-Substituted 1H-Tetrazoles from Nitriles by Continuous Flow: Application to the Synthesis of Valsartan in 2020, Cited 46. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3.

An efficient continuous flow process for the synthesis of 5-substituted 1H-tetrazoles is described. The process involves the reaction between a polymer-supported triorganotin azide and organic nitriles. The polymer-supported organotin azide, which is in situ generated with a polystyrene-supported triorganotin alkoxide and trimethylsilylazide, is immobilized in a packed bed reactor. This approach is simple, fast (it takes from 7.5 to 15 min), and guarantees a low concentration of tin residues in the products (<5 ppm). The process was developed to aryl-, heteroaryl-, and also alkylnitriles and was applied for the synthesis of valsartan, an angiotensin II receptor antagonist. About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Carpentier, F; Felpin, FX; Zammattio, F; Le Grognec, E or concate me.. Category: benzodioxans

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

COA of Formula: C8H7NO3. Recently I am researching about INTRAMOLECULAR 1,3-DIPOLAR CYCLOADDITION; SPIROOXINDOLE NATURAL-PRODUCTS; PROTEIN-PROTEIN INTERACTIONS; SCHIFF-BASE MACROCYCLES; CHIRAL SOLVATING AGENTS; DRUG DISCOVERY; ENCAPSULATION; INDOLIZIDINE; RECOGNITION; CAVITANDS, Saw an article supported by the Council of Scientific and Industrial Research (CSIR) New Delhi, IndiaCouncil of Scientific & Industrial Research (CSIR) – India [09/115(0775)/2014 EMR-I]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Prabhakaran, P; Rajakumar, P. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

A convenient and efficient method for the regioselective macrocyclization of triazole bridged spiropyrrolidine-oxindole, and bis-spiropyrrolizidine-oxindole derivatives was accomplished through intra and self-intermolecular [3 + 2] cycloaddition of azomethine ylides. The chalcone isatin precursors 9a-i required for the click reaction were obtained from the reaction of N-alkylazidoisatin 4 and propargyloxy chalcone 8a-i which in turn were obtained by the aldol condensation of propargyloxy salicylaldehyde 6 and substituted methyl ketones 7a-i. The regio- and stereochemical outcome of the cycloadducts were assigned based on 2D NMR and confirmed by single crystal XRD analysis. High efficiency, mild reaction conditions, high regio- and stereoselectivity, atom economy and operational simplicity are the exemplary advantages of the employed macrocyclization procedure.

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

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

An article CAN-mediated Oxidative Coupling-Reaction of Xanthenes with Enaminones WOS:000596864300001 published article about C-H ACTIVATION; CERIUM(IV) AMMONIUM-NITRATE; BOND ARYLATION; METAL-FREE; MECHANISTIC INSIGHT; MOLECULAR-OXYGEN; HIGHLY EFFICIENT; CROSS; TETRAHYDROISOQUINOLINES; SP(3) in [Zhang, Changyuan; Qiu, Yun; Chen, Lulu; Xu, Shuting; Guo, Huosheng; Luo, Jian; Tan, Yao] Yichun Univ, Jiangxi Univ Appl Chem & Chem Biol, Coll Chem & Bioengn, Key Lab, 576 Xuefu Rd, Yichun 336000, Peoples R China; [Zhang, Jiantao] Guangdong Univ Petrochem Technol, Coll Chem, Guandu Rd, Maoming 525000, Peoples R China in 2021.0, Cited 63.0. 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

An efficient CAN-mediated C-C bond formation in the oxidative reactions of xanthenes with enaminones under mild reaction conditions are described. A variety of 9H-xanthene-9-ylidene aldehydes could be synthesized in up to 90% yield via one-pot manner with good functional group compatibility, which achieved the simultaneous construction of carbon-carbon double bond and carbon-oxygen double bond.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Zhang, CY; Qiu, Y; Zhang, JT; Chen, LL; Xu, ST; Guo, HS; Luo, J; Tan, Y or concate me.. Quality Control of 1-(4-Nitrophenyl)ethanone

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

In 2019.0 J ENZYM INHIB MED CH published article about IRON SUPEROXIDE-DISMUTASE; TRYPANOSOMA-CRUZI; OPTIMIZATION; PROTEIN; ASSAYS; IDENTIFICATION; DENATURATION; CYTOTOXICITY; CALORIMETRY; STABILITY in [Bitencourt Brito, Camila C.; Castilho, Marcelo Santos] Univ Estadual Feira de Santana, Programa Posgrad Biotecnol, Feira De Santana, BA, Brazil; [Carneiro da Silva, Helder Vinicius; Ximenes, Rafael Matos; de Albuquerque, Julianna F. C.] Univ Fed Pernambuco, Dept Antibiot, Recife, PE, Brazil; [Brondanic, Daci Jose; de Faria, Antonio Rodolfo] Univ Fed Pernambuco, Dept Farm, Recife, PE, Brazil; [da Silva, Ivanildo Mangueira] Fac Belo Jardim, Recife, PE, Brazil; [Castilho, Marcelo Santos] Univ Fed Bahia, Fac Farm, Salvador, BA, Brazil in 2019.0, Cited 46.0. 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

Leishmaniasis is considered as one of the major neglected tropical diseases due to its magnitude and wide geographic distribution. Leishmania braziliensis, responsible for cutaneous leishmaniasis, is the most prevalent species in Brazil. Superoxide dismutase (SOD) belongs to the antioxidant pathway of the parasites and human host. Despite the differences between SOD of Leishmania braziliensis and human make this enzyme a promising target for drug development efforts. No medicinal chemistry effort has been made to identify LbSOD inhibitors. Herein, we show that thermal shift assays (TSA) and fluorescent protein-labeled assays (FPLA) can be employed as primary and secondary screens to achieve this goal. Moreover, we show that thiazole derivatives bind to LbSOD with micromolar affinity.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Brito, CCB; da Silva, HVC; Brondanic, DJ; de Faria, AR; Ximenes, RM; da Silva, IM; de Albuquerque, JFC; Castilho, MS or concate me.. Quality Control of 1-(4-Nitrophenyl)ethanone

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

Formula: C8H7NO3. Vargas-Durazo, J; Aguilar-Martinez, M; Ochoa-Teran, A; Santacruz-Ortega, H; Alonzo, FR; Meza, NG; Galvez-Ruiz, JC in [Vargas-Durazo, Judas; Santacruz-Ortega, Hisila] Univ Sonora, Dept Invest Polimeros & Mat, Hermosillo 83000, Sonora, Mexico; [Aguilar-Martinez, Milagros] Univ Sonora, Unidad Reg Norte, Dept Ciencias Quim Biol & Agr, Caborca 83600, Sonora, Mexico; [Ochoa-Teran, Adrian] Tecnol Nacl Mexico, Inst Tecnol Tijuana, Ctr Grad & Invest Quim, Tijuana 22430, Baja California, Mexico; [Rocha Alonzo, Fernando; Carlos Galvez-Ruiz, Juan] Univ Sonora, Dept Ciencias Quim Biol, Hermosillo 83000, Sonora, Mexico; [Gamez Meza, Nohemi] Univ Sonora, Dept Invest Cient & Tecnol, Hermosillo 83000, Sonora, Mexico published Stereoselective Reducing Complexes Supported in Solid Phase: Preparation and Reactivity Study in 2019.0, Cited 24.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Twelve new chiral chelating resins have been prepared using solid phase organic synthesis with the Merrifield and Wang resins and the bidentate amine 1,2-ethylenediamine, followed by the coupling of asymmetric ketones such as 1-phenyletanone, 4-methyl-2-pentanone 4-nitroacetophenone and 4-methoxyacetophenone to form prochiral imines. The enantioselective reduction with borane and (R)-(+)-2-Methyl-CBS-oxazaborolidine leads to the chiral resins with yields greater than 86%. We used these chiral resins to prepare 24 reducing complexes with alkali tetrahydroborates in a very simple way giving yields greater than 87%. Finally, we achieved a preliminary enantioselective reduction of acetophenone employing the Merrifield’s chiral chelating resins obtaining the corresponding S alcohol in a 70:30 ratio with the R analog alcohol.

Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Vargas-Durazo, J; Aguilar-Martinez, M; Ochoa-Teran, A; Santacruz-Ortega, H; Alonzo, FR; Meza, NG; Galvez-Ruiz, JC or concate me.

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

Computed Properties of C8H7NO3. In 2020.0 ASIAN J ORG CHEM published article about ALPHA-AMINO-ACIDS; CARBOLINE DERIVATIVES; GAMMA-CARBOLINE; TANDEM REACTION; INDOLE; AMINATION; STRATEGY in [Yang, Tang-Hao; Kavala, Veerababurao; Kuo, Chun-Wei; Yao, Ching-Fa] Natl Taiwan Normal Univ, Dept Chem, Taipei, Taiwan in 2020.0, Cited 39.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The present methodology describes a versatile pathway to furnish alpha-carbolines from relatively stable 2-amino indole derivatives and 3-bromopropenal. High substrate tolerance, nonmetallic, more efficient, and mild reaction conditions are important aspects.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yang, TH; Kavala, V; Kuo, CW; Yao, CF or concate me.

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

An article Synthesis and molecular docking study of pyrazole clubbed oxazole as antibacterial agents WOS:000577042700001 published article about ANTIMICROBIAL ACTIVITY; BIOLOGICAL EVALUATION; ACCURATE DOCKING; GLIDE; BENZIMIDAZOLE; DERIVATIVES; DESIGN in [Desai, Nisheeth C.; Vaja, Darshita V.; Joshi, Surbhi B.] Maharaja Krishnakumarsinhji Bhavnagar Univ, Div Med Chem, Dept Chem DST FIST & UGC NON SAP, Mahatma Gandhi Campus, Bhavnagar 364002, Gujarat, India; [Khedkar, Vijay M.] Vishwakarma Univ, Dept Pharmaceut Chem, Sch Pharm, Pune 411048, Maharashtra, India in 2021.0, Cited 20.0. Safety 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

We have developed a simple synthetic protocol for the preparation of novel 3-(3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)-5-arylisoxazoles. The structure of synthesized compounds was elucidated by spectral techniques like FT-IR,H-1-NMR,C-13-NMR, and mass. The novel bioactive compounds3a-twere evaluated for in vitro antibacterial activity on several bacterial species. Compounds3c(-4-NO2),3o(-4-F), and3r(-3,4-Cl-2) exhibited good in vitro antibacterial activity. Furthermore, molecular docking on DNA gyrase subunit bcould shed some light on the mechanism of action which can serve as a guide for lead optimization. Graphic abstract

Safety of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Desai, NC; Vaja, DV; Joshi, SB; Khedkar, VM or concate me.

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

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

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