The Shocking Revelation of 1-(4-Nitrophenyl)ethanone

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Ravi, K; Advani, JH; Bankar, BD; Singh, AS; Biradar, AV or concate me.

An article Sustainable route for the synthesis of flower-like Ni@N-doped carbon nanosheets from bagasse and its catalytic activity towards reductive amination of nitroarenes with bio-derived aldehydes WOS:000587607600018 published article about ONE-POT SYNTHESIS; HYDROTHERMAL CARBON; NITRO-COMPOUNDS; BIOMASS; HYDROGENATION; NANOPARTICLES; EFFICIENT; STORAGE; SPHERES in [Ravi, Krishnan; Advani, Jacky H.; Bankar, Balasaheb D.; Singh, Amravati S.; Biradar, Ankush V.] CSIR Cent Salt & Marine Chem Res Inst, Inorgan Mat & Catalysis Div, GB Marg, Bhavnagar 364002, Gujarat, India; [Ravi, Krishnan; Advani, Jacky H.; Bankar, Balasaheb D.; Singh, Amravati S.; Biradar, Ankush V.] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, Uttar Pradesh, India in 2020.0, Cited 55.0. Product Details of 100-19-6. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Utilization of abundantly available biomass to develop advanced materials and products has become an utmost priority these days. Herein, we developed a sustainable route for the synthesis of Ni nanoparticles loaded on N-doped carbon nanosheets using underutilized sugarcane bagasse, urea and NiCl2 center dot 6H(2)O as the carbon, nitrogen and Ni source. The synthesized catalyst was characterized using different analytical techniques; FESEM, elemental mapping and HRTEM analysis revealed the formation of flower-like carbon nanosheets containing uniformly distributed nickel nanoparticles with average particle size of 2.4-10 nm. The synthesized nanocatalyst was used for the one-pot reductive amination of different bio-derived aldehydes with the nitroarenes at 100 degrees C for 4 h. The complete conversion of the variety of nitroarenes with the formation of imines and benzimidazole products was obtained under optimized reaction conditions. The catalyst was recyclable up to five times with negligible loss in selectivity towards imines.

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Ravi, K; Advani, JH; Bankar, BD; Singh, AS; Biradar, AV or concate me.

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

An overview of features, applications of compound:100-19-6

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Du, JL; Chen, J; Xia, HH; Zhao, YW; Wang, F; Liu, H; Zhou, WJ; Wang, B or concate me.

I found the field of Chemistry very interesting. Saw the article Commercially Available CuO Catalyzed Hydrogenation of Nitroarenes Using Ammonia Borane as a Hydrogen Source published in 2020.0. Application In Synthesis of 1-(4-Nitrophenyl)ethanone, Reprint Addresses Zhou, WJ (corresponding author), Univ Jinan, Inst Adv Interdisciplinary Res, Collaborat Innovat Ctr Technol & Equipment Biol D, Jinan 250022, Shandong, Peoples R China.; Wang, B (corresponding author), Univ Jinan, Sch Chem & Chem Engn, Jinan 250022, Shandong, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Tandem ammonia borane dehydrogenation and nitroarenes hydrogenation has been reported as a novel strategy for the preparation of aromatic amines. However, the practical application of this strategy is subjected to the high-cost and tedious preparation of supported noble metal nanocatalysts. The commercially available CuO powder is herein demonstrated to be a robust catalyst for hydrogenation of nitroarenes using ammonia borane as a hydrogen source under mild conditions. Numerous amines (even sterically hindered, halogenated, and diamines) could be obtained through this method. This monometallic catalyst is characteristic of support-free, excellent chemoselectivity, low-cost, and high recyclability, which will favor its future utilization in preparative reduction chemistry. Mechanistic studies are also carried out to clarify that diazene and azoxybenzene are key intermediates of this heterogeneous reduction.

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Du, JL; Chen, J; Xia, HH; Zhao, YW; Wang, F; Liu, H; Zhou, WJ; Wang, B or concate me.

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

Interesting scientific research on 100-19-6

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yamamoto, Y; Fukui, M; Tanaka, A; Hashimoto, K; Kominami, H or concate me.

Product Details of 100-19-6. In 2019.0 CATAL SCI TECHNOL published article about LOADED TITANIUM(IV) OXIDE; CHEMOSELECTIVE REDUCTION; ALCOHOLIC SUSPENSIONS; NITROBENZENE; DIOXIDE; EFFICIENT; ALKENES; FUNCTIONALIZATION; CATALYST; ANILINE in [Yamamoto, Yuhei; Fukui, Makoto] Kindai Univ, Interdisciplinary Grad Sch Sci & Engn, Mol & Mat Engn, 3-4-1 Kowakae, Higashiosaka, Osaka 5778502, Japan; [Tanaka, Atsuhiro; Hashimoto, Keiji; Kominami, Hiroshi] Kindai Univ, Dept Appl Chem, Fac Sci & Engn, 3-4-1 Kowakae, Higashiosaka, Osaka 5778502, Japan in 2019.0, Cited 42.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A titanium.IV) oxide photocatalyst modified with 2,3-dihydroxynaphthalene (DHN/TiO2) responds to visible light, and electrons are photogenerated to the conduction band of TiO2 under light irradiation in the presence of a suitable hole scavenger. The reducing potential of DHN/TiO2 was applied for photocatalytic conversion of a nitro group to an amino group of aromatics having other reducible groups under hydrogenfree and noble metal-free conditions at room temperature. Various nitro aromatics having vinyl, chloro, bromo, and acetyl groups were converted to amino aromatics with high yields with the reducible groups being preserved. Some parameters affecting the catalytic performance were investigated, and the reaction rate was almost determined by the amount of the substrate adsorbed on DHN/TiO2.

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yamamoto, Y; Fukui, M; Tanaka, A; Hashimoto, K; Kominami, H or concate me.

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

What about chemistry interests you the most 1-(4-Nitrophenyl)ethanone

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yun, RR; Hong, LR; Ma, WJ; Jia, WG; Liu, SJ; Zheng, BS or concate me.. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

An article Fe/Fe2O3@N-dopped Porous Carbon: A High-Performance Catalyst for Selective Hydrogenation of Nitro Compounds WOS:000459734900011 published article about METAL-ORGANIC FRAMEWORKS; CHEMOSELECTIVE HYDROGENATION; EFFICIENT; NANOPARTICLES; NITROARENES; REDUCTION; DEHYDROGENATION; ALDEHYDES; WATER in [Yun, Ruirui; Hong, Lirui; Ma, Wanjiao; Jia, Weiguo; Liu, Shoujie] Anhui Normal Univ, Key Lab Funct Mol Solids, Minist Educ, Coll Chem & Mat Sci, Wuhu 241000, Peoples R China; [Zheng, Baishu] Hunan Univ Sci & Technol, Key Lab Theoret Organ Chem & Funct Mol, Hunan Prov Key Lab Controllable Preparat & Funct, Minist Educ,Sch Chem & Chem Engn, Xiangtan 411201, Peoples R China in 2019.0, Cited 46.0. Application In Synthesis 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

Herein, we designed and prepared a novel Fe/Fe2O3-based catalyst, in which a remarkable synergistic effect has been revealed between Fe and Fe2O3 encapsulated in N-doping porous carbon. The Fe-based catalysts were fabricated via pyrolysis a mixture of MIL-101(Fe) and melamine. The catalyst exhibits exceptionally high catalytic activity (TOFs up to 8898 h(-1) which is about 100 times higher than the similar kinds of catalysts) and chemoselectivity for nitroarene reduction under mild conditions.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yun, RR; Hong, LR; Ma, WJ; Jia, WG; Liu, SJ; Zheng, BS or concate me.. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

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

The Absolute Best Science Experiment for 100-19-6

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Brand, S; Causero, A; Elsen, H; Pahl, J; Langer, J; Harder, S or concate me.

I found the field of Chemistry very interesting. Saw the article Ligand Effects in Calcium Catalyzed Ketone Hydroboration published in 2020.0. Application In Synthesis of 1-(4-Nitrophenyl)ethanone, Reprint Addresses Harder, S (corresponding author), Univ Erlangen Nurnberg, Inorgan & Organometall Chem, Egerlandstr 1, D-91058 Erlangen, Germany.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The first naked (Lewis base-free) cationic Ca amidinate complex [(AmCa)-Am-tBu-Ca-DIPP(C6H6)](+)[B(C6F5)(4)](-) was prepared in 62 % yield {(AmDIPP)-Am-tBu = tBuC(N-DIPP)(2); DIPP = 2,6-diisopropylphenyl} by reaction of [(AmCaH)-Am-tBu-Ca-DIPP](2) with [Ph3C](+)[B(C6F5)(4)](-) in chlorobenzene. The ether-free complex (AmCaN)-Am-tBu-Ca-DIPP(SiMe3)(2) was obtained by removal of diethyl ether from its ether adduct. Crystal structures show that the amidinate ligand in both complexes is N,Aryl-chelating. In this coordination mode the bulk of the amidinate ligand is comparable to that of a DIPP-substituted beta-diketiminate ligand. Isomers with N,N-coordinating amidinate ligands are circa 15 kcal/mol higher in energy and this coordination mode is only present in case additional ether ligands compensate for energy loss or in case of space limitation at the metal, e.g. in homoleptic (Am-tBu(DIPP))(2)Ca. A series of four Ca amidinate complexes, (AmCaX)-Am-tBu-Ca-DIPP, were tested in the catalytic hydroboration of ketones and aldehydes by pinacolborane (HBpin). Catalytic activities increase for X- = I- < B(C6F5)(4)(-) < (Me3Si)(2)N- approximate to H-. For catalysts with unreactive anions, like I- or B(C6F5)(4)(-), catalyst performance increases with the Lewis acidity of the metal and a mechanism is proposed in which HBpin and ketone coordinate to the Ca2+ ion which is followed by direct hydroboration. The more active catalysts with X- = (Me3Si)(2)N- or H- likely operate through a mechanism which involves intermediate metal hydride (or borate) complexes. Application In Synthesis of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Brand, S; Causero, A; Elsen, H; Pahl, J; Langer, J; Harder, S or concate me.

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

Extended knowledge of 100-19-6

Name: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Han, AJ; Zhang, J; Sun, WM; Chen, WX; Zhang, SL; Hang, YH; Feng, QC; Zheng, LR; Gu, L; Chen, C; Peng, Q; Wang, DS; Li, YD or concate me.

Name: 1-(4-Nitrophenyl)ethanone. Recently I am researching about METAL-SUPPORT INTERACTION; ACTIVE-SITES; PD-GA; CATALYSTS; METHANOL; SURFACE; SIZE; CO; SEMIHYDROGENATION; NANOSTRUCTURES, Saw an article supported by the China Ministry of Science and TechnologyMinistry of Science and Technology, China [0202801]; National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21521091, 21390393, U1463202, 21471089, 21671117, 21703219, 21521005]; 111 ProjectMinistry of Education, China – 111 Project [B16028]. Published in NATURE RESEARCH in BERLIN ,Authors: Han, AJ; Zhang, J; Sun, WM; Chen, WX; Zhang, SL; Hang, YH; Feng, QC; Zheng, LR; Gu, L; Chen, C; Peng, Q; Wang, DS; Li, YD. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

Noble metals play a momentous role in heterogeneous catalysis but still face a huge challenge in selectivity control. Herein, we report isolating contiguous Pt atoms and forming Pt-Zn intermetallic nanoparticles as an effective strategy to optimize the selectivity of Pt catalysts. Contiguous Pt atoms are isolated into single atoms and Pt-Zn intermetallic nanoparticles are formed which are supported on hollow nitrogen-doped carbon nanotubes (PtZn/HNCNT), as confirmed by aberration-corrected high-resolution transmission electron microscopy and X-ray absorption spectrometry measurements. Interestingly, this PtZn/HNCNT catalyst promotes the hydrogenation of 4-nitrophenylacetylene to 4-aminophenylacetylene with a much higher conversion (> 99%) and selectivity (99%) than the comparison samples with Pt isolated-single-atomic-sites (Pt/HNCNT) and Pt nanoparticles (Pt/CN). Further density functional theory (DFT) calculations disclose that the positive Zn atoms assist the adsorption of nitro group and Pt-Zn intermetallic nanoparticles facilitate the hydrogenation on nitro group kinetically.

Name: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Han, AJ; Zhang, J; Sun, WM; Chen, WX; Zhang, SL; Hang, YH; Feng, QC; Zheng, LR; Gu, L; Chen, C; Peng, Q; Wang, DS; Li, YD or concate me.

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

How did you first get involved in researching C8H7NO3

HPLC of Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Oliveira, RL; Ben Ghorbel, MC; Praetz, S; Meiling, D; Schlesiger, C; Schomacker, R; Thomas, A or concate me.

I found the field of Chemistry; Science & Technology – Other Topics; Engineering very interesting. Saw the article Confinement of Cobalt Species in Mesoporous N-Doped Carbons and the Impact on Nitroarene Hydrogenation published in 2020.0. HPLC of Formula: C8H7NO3, Reprint Addresses Oliveira, RL; Thomas, A (corresponding author), Tech Univ Berlin, Fak 2, Inst Chem Funkt Mat, D-10623 Berlin, Germany.; Oliveira, RL (corresponding author), Tech Univ Berlin, Fak 2, Inst Chem, D-10623 Berlin, Germany.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

A general strategy to synthesize mesoporous and macroporous carbon and N-doped mesoporous carbon is presented. The immobilization of cobalt catalysts with dispersed subnanometer particles in mesoporous N-doped carbon matrixes is also shown. These materials were used as catalysts for the hydrogenation of nitroarenes under considerably mild conditions. The surface area and the presence of nitrogen on the supports were demonstrated to be fundamental to disperse and stabilize the active metal species, which were responsible for the outstanding performance of these materials compared to cobalt catalysts deposited on silica, alumina, or mesoporous carbon. Finally, the ability to catalyze the hydrogenation of nitroarenes containing electron-donating groups (EDGs) and electron-withdrawing groups (EWGs) with good selectivity was also explored.

HPLC of Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Oliveira, RL; Ben Ghorbel, MC; Praetz, S; Meiling, D; Schlesiger, C; Schomacker, R; Thomas, A or concate me.

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

Extracurricular laboratory: Synthetic route of 1-(4-Nitrophenyl)ethanone

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Hosseini-Sarvari, M; Akrami, Z or concate me.

An article Visible-light assisted of nano Ni/g-C3N4 with efficient photocatalytic activity and stability for selective aerobic C-H activation and epoxidation WOS:000588151800009 published article about GRAPHITIC CARBON NITRIDE; OXIDATION; ALKENES; NANOCOMPOSITE; EVOLUTION; CATALYSTS; STYRENE; DRIVEN; WATER; ZNO in [Hosseini-Sarvari, Mona; Akrami, Zahra] Shiraz Univ, Fac Sci, Dept Chem, Shiraz 7194684795, Iran in 2020.0, Cited 53.0. 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

A selective, economical, and ecological protocol has been described for the oxidation of methyl arenes and their analogs to the corresponding carbonyl compounds and epoxidation reactions of alkenes with molecular oxygen (O-2) or air as a green oxygen source, under mild reaction conditions. The nano Ni/g-C3N4 exhibited high photocatalytic activity, stability, and selectivity in the C-H activation of methyl arenes, methylene arenes, and epoxidation of various alkenes under visible- light irradiation without the use of an oxidizing agent and under base free conditions. (C) 2020 Elsevier B.V. All rights reserved.

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Hosseini-Sarvari, M; Akrami, Z or concate me.

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

Some scientific research about 1-(4-Nitrophenyl)ethanone

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Liu, Y; Lv, MX; Li, L; Yu, HL; Wu, Q; Pang, JH; Liu, YX; Xie, CX; Yu, ST; Liu, SW or concate me.. Quality Control of 1-(4-Nitrophenyl)ethanone

Quality Control of 1-(4-Nitrophenyl)ethanone. I found the field of Chemistry very interesting. Saw the article Synthesis of a highly active amino-functionalized Fe3O4@SiO2/APTS/Ru magnetic nanocomposite catalyst for hydrogenation reactions published in 2019.0, Reprint Addresses Yu, ST; Liu, SW (corresponding author), Qingdao Univ Sci & Technol, Coll Chem Engn, 53 Zhengzhou Rd, Qingdao 266042, Shandong, Peoples R China.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.

An amino-functionalized silica-coated Fe3O4 nanocomposite (Fe3O4@SiO2/APTS) was synthesized. The Fe3O4@SiO2 microspheres possessed a well-defined core-shell structure, uniform sizes and high magnetization. An immobilized ruthenium nanoparticle catalyst (Fe3O4@SiO2/APTS/Ru) was obtained after coordination and reduction of Ru3+ on the Fe3O4@SiO2/APTS nanocomposite. The Ru nanoparticles were not only ultra-small with nearly monodisperse sizes but also had strong affinity with the surface of Fe3O4@SiO2/APTS. The obtained catalyst exhibited excellent catalytic performance for the hydrogenation of a variety of aromatic nitro compounds, even at room temperature. Moreover, Fe3O4@SiO2/APTS/Ru was easily recovered using a magnetic field and directly reused for at least five cycles without significant loss of its activity.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Liu, Y; Lv, MX; Li, L; Yu, HL; Wu, Q; Pang, JH; Liu, YX; Xie, CX; Yu, ST; Liu, SW or concate me.. Quality Control of 1-(4-Nitrophenyl)ethanone

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

What unique challenges do researchers face in 100-19-6

SDS of cas: 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact de Melo, SCG; da Silva, MEP; da Silva, MEB; da Paz, JA; Barbosa, CMBD; de Menezes, FD; Loureiro, RNA; Navarro, M; da Costa, JAP; da Silva, GF; Villa, AAO; Vilar, M or concate me.

In 2020.0 INT J HYDROGEN ENERG published article about ORGANIC-COMPOUNDS; CARBONYL-COMPOUNDS; ENANTIOSELECTIVE HYDROGENATION; ELECTROCHEMICAL HYDROGENATION; CHEMOSELECTIVE HYDROGENATION; GRAPHENE NANOSHEETS; BETA-CYCLODEXTRIN; GREEN CHEMISTRY; DESIGN ANALYSIS; SCALE-UP in [Galvao de Melo, Sarah Calado; Pereira da Silva, Maria Eduarda; Barreto da Silva, Maria Eduarda; de Menezes, Frederico Duarte; Albert Loureiro, Rodrigo Nogueira; Peixoto da Costa, Jose Angelo; Ochoa Villa, Alvaro Antonio; Vilar, Marcio] Inst Fed Educ Ciencia & Tecnol Pernambuco, Dept Sistemas Proc & Controles Ind, BR-50740540 Recife, PE, Brazil; [da Paz, Josinete Angela; Navarro, Marcelo] Univ Fed Pernambuco, Dept Quim Fundamental, BR-50670901 Recife, PE, Brazil; [Bezerra de Menezes Barbosa, Celmy Maria] Univ Fed Pernambuco, Dept Engn Quim, BR-50740521 Recife, PE, Brazil; [da Silva, Gabriel Francisco] Univ Fed Sergipe, Dept Quim, BR-49100000 Sao Cristovao, SE, Brazil in 2020.0, Cited 107.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. SDS of cas: 100-19-6

Benzylic alcohols have an important role in organic synthesis as target molecules of biological interest, which can be produced from the reduction of aromatic carbonyl substrates. In this work, the sonoelectrocatalytic hydrogenation (SECH) of aryl ketones was studied in water. The ultrasonic irradiation was carried out at frequency of 20 kHz +/- 500 Hz with a cylindrical titanium probe (MS 73 microtip; Ti-6AI-4V alloy; 3.0 mm diameter; Pacoustic- = 2.11 W). The results showed that the ultrasound irradiation enhances the mass-transport of the substrates from the bulk solution to the electrode surface, increasing the substrate availability to react with the adsorbed H, leading to higher yields. Regarding the electrode material, the following hydrogenation yields of a group of acetophenones was observed: Cu (79.0 +/- 1.5%) > Ni (73.0 +/- 2.0%) approximate to Fe/Ni (72.0 +/- 1.7%) > graphite (69.0 +/- 1.7%) > Fe (67.5 +/- 2.3%). The SECH presented a slight variation in the reactivity of some reagents, and its behaviour depends on the catalytic nature of the electrode support. Besides the lower overpotential and higher exchange current density of the graphite, it was surprisingly active under ultrasound irradiation, showing higher yields and current efficiencies than others electrocatalytic hydrogenation (ECH) procedures. The ultrasound irradiation decreases more than 6-folds the energy consumption of the ECH method, making it an effective and inexpensive way to produce alcohols from the respective aryl ketones in water. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

SDS of cas: 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact de Melo, SCG; da Silva, MEP; da Silva, MEB; da Paz, JA; Barbosa, CMBD; de Menezes, FD; Loureiro, RNA; Navarro, M; da Costa, JAP; da Silva, GF; Villa, AAO; Vilar, M or concate me.

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