Month: November 2021

In 2021.0 CHEMCATCHEM published article about LAYERED DOUBLE HYDROXIDE; CATALYZED ALPHA-ALKYLATION; RUTHENIUM-GRAFTED HYDROTALCITE; BAEYER-VILLIGER OXIDATION; NICKEL-IRON HYDROTALCITE; EFFICIENT CATALYSTS; ACCEPTORLESS DEHYDROGENATION; 2-AMINOBENZYL ALCOHOL; AEROBIC OXIDATION; MOLECULAR-OXYGEN in [Motokura, Ken; Ozawa, Nao; Manaka, Yuichi] Tokyo Inst Technol, Sch Mat & Chem Technol, Dept Chem Sci & Engn, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268502, Japan; [Motokura, Ken] Japan Sci & Technol Agcy JST, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan; [Manaka, Yuichi] Natl Inst Adv Ind Sci & Technol, Renewable Energy Res Ctr, 2-2-9 Machiikedai, Koriyama, Fukushima 9630298, Japan; [Chun, Wang-Jae] Int Christian Univ, Grad Sch Arts & Sci, Mitaka, Tokyo 1818585, Japan; [Motokura, Ken] Yokohama Natl Univ, Dept Chem & Life Sci, Hodogaya Ku, 79-5 Tokiwadai, Yokohama, Kanagawa 2408501, Japan in 2021.0, Cited 86.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Name: 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.

Name: 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

Recommanded Product: 100-19-6. Authors Fu, Y; Yang, CY; Zheng, YT; Jiang, JW; Sun, Y; Chen, F; Hu, JS in ELSEVIER published article about in [Fu, Yong; Yang, Chengyue; Zheng, Yutong; Jiang, Jinwen; Sun, Yu; Hu, Jianshe] Northeastern Univ, Coll Sci, Ctr Mol Sci & Engn, Shenyang 110819, Peoples R China; [Chen, Feng] Ningde Normal Univ, Fujian Prov Univ Key Lab Green Energy & Environm, Coll Chem & Mat, Fujian Prov Key Lab Featured Mat Biochem Ind, Ningde 352100, Fujian, Peoples R China in 2021.0, Cited 44.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Elemental sulfur, as a by-product of petroleum refining, is regarded as a solid waste stored in above-ground deposits due to limited existing applications, meanwhile, mercury contamination is one of the current environmental issues considering its high toxicity to the human, and how to safely dispose of hazardous waste adsorbents is still an unavoidable problem. This study addresses these need by utilizing sulfur for preparation of a polysulfide complex material to capture Hg(II) and convert the Hg(II)-containing spent adsorbent into a catalyst. Initially, the mesoporous silica was prepared and functionalized by using diatomite and APTES, then, an in-situ preparation method was applied to obtain the amine-mesoporous silica/poly(m-aminothiophenol) nanocomposite (MAP), subsequently sulfur was copolymerized with MAP and vinylic-potato starch through inverse vulcanization, forming the sulfur crosslinked polymers composite cp(MAP-S-PS). Many characterizations were employed to determine the physicochemical structure andmorphology of cp(MAP-S-PS). The adsorption study showed the cp(MAP-S-PS) exhibited the theoretical maximum adsorption capacity of 436.68 mg/g, good regeneration performance after 5 cycles and excellent selectivity between Hg(II) ions and common cations. Furthermore, the collected spent adsorbent cp (MAP-S-PS)/Hg(II) was reused as a catalyst for synthesis of acetophenone with 89% yield, and most of phenylacetylene derivatives were also transformed to corresponding acetophenone in good yields. (C) 2021 Published by Elsevier B.V.

Welcome to talk about 100-19-6, If you have any questions, you can contact Fu, Y; Yang, CY; Zheng, YT; Jiang, JW; Sun, Y; Chen, F; Hu, JS or send Email.. Recommanded Product: 100-19-6

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

An article Sterically hindered N-heterocyclic carbene/palladium(ii) catalyzed Suzuki-Miyaura coupling of nitrobenzenes WOS:000478612600005 published article about PALLADIUM; COMPLEXES; NICKEL; NITROARENES; CONVERSION; CARBENES; ELECTROPHILES; AMINATION; CALCIUM; ESTERS in [Chen, Kai; Chen, Wei; Yi, Xiaofei; Chen, Wanzhi] Zhejiang Univ, Dept Chem, 38 Zheda Rd, Hangzhou 310027, Zhejiang, Peoples R China; [Liu, Miaochang; Wu, Huayue] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325027, Peoples R China 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

Palladium-catalyzed denitrative Suzuki coupling of nitroarenes using 2-aryl-5-(2,4,6-triisopropylphenyl)-2,3-imidazolylidene[1,5-a]pyridines as the ligands is described. The key to success is the use of the NHC ligands which show strong donating ability and suitable steric hindrance allowing the successful oxidative addition of Ar-NO2 bonds. Both aromatic and aliphatic boronic acids are tolerated, and a variety of biphenyls and alkylarenes were obtained in good to excellent yields.

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.. Quality Control of 1-(4-Nitrophenyl)ethanone

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

Recommanded Product: 100-19-6. In 2019.0 CATAL LETT published article about ASYMMETRIC TRANSFER HYDROGENATION; RUTHENIUM(II) COMPLEXES; MONTMORILLONITE K-10; IRON NANOPARTICLES; FURFURYL ALCOHOL; LIGANDS; EPOXIDATION; OXIDATION; REDUCTION; IRIDIUM in [Sultana, Samim; Borah, Geetika; Gogoi, Pradip. K.] Dibrugarh Univ, Dept Chem, Dibrugarh, Assam, India in 2019.0, Cited 76.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A new Fe(II) Schiff base complex anchored on mont-K10 (Fe@imine-mont-K10) was synthesized and extensively characterized by FTIR, powder X-ray diffraction, SEM-EDX, TEM, ESR, X-ray photoelectron spectroscopy (XPS), BET surface area measurement, solid state Si-29 NMR and ICP-AES analysis. The catalytic activity of the complex was investigated for hydrogenation of ketones. The results indicated that it exhibited good catalytic activity for hydrogenation of aromatic as well as aliphatic ketones in i-PrOH/CH3CN (1:1) using Na-i-OPr as base at 80 degrees C resulting in moderate to excellent isolated yields (51-99%) of their corresponding products. The catalyst shows good reusability. [GRAPHICS] .

Welcome to talk about 100-19-6, If you have any questions, you can contact Sultana, S; Borah, G; Gogoi, PK or send Email.. Recommanded Product: 100-19-6

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

Authors El-sayed, HA; Assy, MG; Mohamed, AS in WILEY-V C H VERLAG GMBH published article about in [El-sayed, Hassan A.; Assy, Mohamed G.; Mohamed, Asaad S.] Zagazig Univ, Fac Sci, Dept Chem, Zagazig 44519, Egypt in 2019.0, Cited 15.0. HPLC of Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

An efficient and facile approach has been described for the synthesis of a new series of 1-amino-2-oxo-nicotinonitriles and their sulfonamides under microwave and ultrasonic irradiation. The desired compounds 4 a-l were obtained via condensation of p-chlorobenzaldehyde, aryl or heteroaryl methyl ketone and cyanoacetohydrazide in the presence of catalytic piperidine under three synthetic methodologies (namely, conventional method, ultrasonic and microwave irradiation), the best results (short reaction times, pure products, high yield) were obtained by ultrasonic irradiation. Sulfonamides 5 a-f resulted via reaction of amines 4 a-e and 4 j with benzene sulfonyl chloride in the presence of pyridine. The synthesized compounds give no significant results when investigated against Gm (+ve) and Gm (-ve) bacteria, and fungi strains.

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

An article Visible-Light-Promoted Switchable Synthesis of C-3-Functionalized Quinoxalin-2(1H)-ones WOS:000609298500001 published article about SINGLET OXYGEN; DECARBOXYLATIVE ACYLATION; PHOTOSENSITIZED OXIDATION; PHOTOREDOX CATALYSIS; METAL; DESIGN; FUNCTIONALIZATION; QUINOXALINONES; INHIBITORS; SULFOXIDES in [Aganda, Kim Christopher C.] Myongji Univ, Dept Energy Sci & Technol, Yongin 17058, South Korea; [Hong, Boseok] Myongji Univ, Dept Chem, Yongin 17058, South Korea; [Aganda, Kim Christopher C.; Lee, Anna] Jeonbuk Natl Univ, Dept Chem, Jeonju 54896, South Korea in 2021.0, Cited 60.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A visible-light-promoted synthesis of quinoxalin-2(1H)-ones has been developed using 9-mesityl-10-methylacridinium perchlorate as an organo-photocatalyst. The atmosphere-controlled method (Ar/air) enabled the selective synthesis of hydroxyl- and acyl-containing quinoxalin-2(1H)-ones under mild reaction conditions without the use of any metal catalysts or toxic reagents. A fluorescent labelling experiment showed that hydroxyl-containing quinoxalin-2(1H)-ones may have utility in various biological applications as potent fluorophores.

Category: benzodioxans. 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

Authors Venkatesh, N; Sundergoud, S; Swamy, MK; Veerasomaiah, P in MAIK NAUKA/INTERPERIODICA/SPRINGER published article about DERIVATIVES; DISCOVERY; APOPTOSIS in [Venkatesh, N.; Sundergoud, Sh.; Swamy, M. Kumara; Veerasomaiah, P.] Osmania Univ, Univ Coll Sci, Dept Chem, Hyderabad 500007, Andhra Pradesh, India in 2020.0, Cited 25.0. Computed Properties of C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A simple and efficient microwave-assisted protocol has been developed for the synthetic of a series of novel pyrazole-indanone hybrid analogs. The target compounds have been synthesized by the Claisen-Schmidt condensation of different 1,3-diphenyl-1H-pyrazole-4-carbaldehydes with 2,3-dihydro-1H-inden-1-one in the presence of potassium hydroxide. The compounds were characterized by IR,H-1 and(13)C NMR, and mass spectra and were found to exhibit potent antimicrobial activity in vitro.

Welcome to talk about 100-19-6, If you have any questions, you can contact Venkatesh, N; Sundergoud, S; Swamy, MK; Veerasomaiah, P or send Email.. Computed Properties of C8H7NO3

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

Recommanded Product: 1-(4-Nitrophenyl)ethanone. In 2019.0 EUR J ORG CHEM published article about ESTERS; HYDROBORATION; BORYLATION; ALKYNES; DIVERSIFICATION; CARBANIONS in [Kovalenko, Maksym; Yarmoliuk, Dmytro, V; Serhiichuk, Dmytro; Chernenko, Dania; Smyrnov, Vladyslav; Breslayskyi, Artur; Hryshchuk, Oleksandr, V; Kleban, Ihor; Tymtsunik, Andriy, V; Tolmachev, Andrey A.; Kuchkovska, Yuliya O.; Grygorenko, Oleksandr O.] Enamine Ltd, Chervonotkatska St 78, UA-02094 Kiev, Ukraine; [Yarmoliuk, Dmytro, V; Smyrnov, Vladyslav; Hryshchuk, Oleksandr, V; Tolmachev, Andrey A.; Kuchkovska, Yuliya O.; Grygorenko, Oleksandr O.] Tams Shevchenko Natl Univ Kyiv, Volodymyrska St 60, UA-01601 Kiev, Ukraine; [Kleban, Ihor; Rassukana, Yuliya] Natl Acad Sci Ukraine, Inst Organ Chem, Murmanska St 5, UA-02660 Kiev, Ukraine; [Chernenko, Dania; Rassukana, Yuliya; Tymtsunik, Andriy, V] Natl Tech Univ Ukraine, Igor Sikorsky Kyiv Polytech Inst, Prospect Perem 37, UA-03056 Kiev, Ukraine 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.

Preparation of 2,2-disubstituted and 2-monosubstituted alkenylboronic acid esters from aliphatic and aromatic ketones and aldehydes by the boron-Wittig olefination with bis[(pinacolato)boryl]methane was examined and applied on the multigram scale. The influence of the substrate steric and electronic features on the overall efficiency and stereochemical outcome of the reaction was studied. Additionally, a series of diversely functionalized (hetera)cycloalkylidenemethyl and (hetera)cycloalkyl boronic acid-derived building blocks was synthesized.

Welcome to talk about 100-19-6, If you have any questions, you can contact Kovalenko, M; Yarmoliuk, DV; Serhiichuk, D; Chernenko, D; Smyrnov, V; Breslayskyi, A; Hryshchuk, OV; Kleban, I; Rassukana, Y; Tymtsunik, AV; Tolmachev, AA; Kuchkovska, YO; Grygorenko, OO or send Email.. Recommanded Product: 1-(4-Nitrophenyl)ethanone

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

Recently I am researching about CATALYZED SYNTHESIS; HYDRAZOIC ACID; CHEMISTRY; TETRAZOLES; REAGENTS; SAFE; CYCLOADDITION; SALTS, Saw an article supported by the University of Nantes; Centre National de la Recherche Scientifique (CNRS)Centre National de la Recherche Scientifique (CNRS); Societe d’Acceleration du Transfert de Technologies Ouest Valorisation. Product Details of 86-29-3. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Carpentier, F; Felpin, FX; Zammattio, F; Le Grognec, E. The CAS is 86-29-3. Through research, I have a further understanding and discovery of 2,2-Diphenylacetonitrile

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. Product Details of 86-29-3. About 2,2-Diphenylacetonitrile, If you have any questions, you can contact Carpentier, F; Felpin, FX; Zammattio, F; Le Grognec, E or concate me.

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

COA of Formula: C8H7NO3. Recently I am researching about CHEMOSELECTIVE HYDROGENATION; ELECTRON-TRANSFER; REDUCTION; GRAPHENE; CARBON; CATALYSTS; GRAPHITE; POLYMER; KETONES, Saw an article supported by the JST CRESTJapan Science & Technology Agency (JST)Core Research for Evolutional Science and Technology (CREST) [JPMJCR18R3]; JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [19H02718]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Ahmad, MS; He, HX; Nishina, Y. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The selective hydrogenation of the nitro moiety is a difficult task in the presence of other reducible functional groups such as alkenes or alkynes. We show that the carbon-based (metal-free) catalyst can be used to selectively reduce substituted nitro groups using H-2 as a reducing agent, providing a great potential to replace noble-metal catalysts and contributing to simple and greener strategies for organic synthesis.

COA of Formula: C8H7NO3. Welcome to talk about 100-19-6, If you have any questions, you can contact Ahmad, MS; He, HX; Nishina, Y or send Email.

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