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

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

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

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

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

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

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

Chemistry Milestones Of 1-(4-Nitrophenyl)ethanone

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yan, XL; Duan, P; Zhang, FW; Li, H; Zhang, HX; Zhao, M; Zhang, XM; Xu, BS; Pennycook, SJ; Guo, JJ or concate me.. HPLC of Formula: C8H7NO3

In 2019.0 CARBON published article about LIQUID-PHASE HYDROGENATION; TRANSITION-METAL CR; P-CHLORONITROBENZENE; NANOPARTICLES; CO; OXIDATION; EFFICIENT; MN; FE; NI in [Yan, Xiaoli; Duan, Pei; Li, Hai; Zhang, Haixia; Zhao, Min; Xu, Bingshe; Guo, Junjie] Taiyuan Univ Technol, Minist Educ, Key Lab Interface Sci & Engn Adv Mat, Taiyuan 030024, Shanxi, Peoples R China; [Zhang, Fengwei; Zhang, Xianming] Shanxi Univ, Inst Crystalline Mat, Taiyuan 030006, Shanxi, Peoples R China; [Pennycook, Stephen J.] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117575, Singapore in 2019.0, Cited 40.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. HPLC of Formula: C8H7NO3

Supported platinum (Pt) catalysts present excellent chemoselectivity for a variety of hydrogenation reactions. Minimizing the use of such expensive catalysts while retaining their catalytic activities has been one of the most challenging topics in recent years. The construction of well dispersed, stable Pt single atom catalysts both increases the density of catalytically active sites while reducing Pt usage. Here we report the synthesis of Pt single atoms trapped in carbon onion graphitic shells by arc-discharge in aqueous solution. Such graphitic shells not only limit the chemical/thermal coarsening of Pt single atoms, but also enhance the conductivity for accelerating the penetration and exchange of ions and electrons during the catalytic process. Experimental results demonstrate that the Pt single atomcatalysts show superior performance and no detectable loss of activity and selectivity over 10 cycles (both remain >99%) for the hydrogenation of p-chloronitrobenzene. This novel atomically dispersed form of Pt catalyst is indicative of a new avenue towards efficient synthesis of single atom catalysts with improved performance. (C) 2018 Elsevier Ltd. All rights reserved.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yan, XL; Duan, P; Zhang, FW; Li, H; Zhang, HX; Zhao, M; Zhang, XM; Xu, BS; Pennycook, SJ; Guo, JJ or concate me.. HPLC of Formula: C8H7NO3

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

Simple exploration of C8H7NO3

Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Sarki, N; Goyal, V; Tyagi, NK; Puttaswamy; Narani, A; Ray, A; Natte, K or concate me.

Category: benzodioxans. In 2021.0 CHEMCATCHEM published article about ALCOHOLS in [Sarki, Naina; Goyal, Vishakha; Tyagi, Nitin Kumar; Narani, Anand; Ray, Anjan; Natte, Kishore] CSIR Indian Inst Petr, Chem & Mat Sci Div, Haridwar Rd, Dehra Dun 248005, Uttarakhand, India; [Sarki, Naina; Goyal, Vishakha; Natte, Kishore] Acad Sci & Innovat Res AcSIR, CSIR HRDC Campus,Joggers Rd, Ghaziabad 201002, Uttar Pradesh, India; [Narani, Anand] CSIR Indian Inst Petr CSIR IIP, BioFuels Div, Haridwar Rd, Dehra Dun 248005, Uttarakhand, India; [Ray, Anjan] CSIR Indian Inst Petr CSIR IIP, Analyt Sci Div, Haridwar Rd, Dehra Dun 248005, Uttarakhand, India; [Puttaswamy] Bangalore Univ, Dept Chem, Jnana Bharathi Campus, Bangalore 560056, Karnataka, India in 2021.0, Cited 148.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Methanol is a potential hydrogen source and C-1 synthon, which finds interesting applications in both chemical synthesis and energy technologies. The effective utilization of this simple alcohol in organic synthesis is of central importance and attracts scientific interest. Herein, we report a clean and cost-competitive method with the use of methanol as both C-1 synthon and H-2 source for selective N-methylation of amines by employing relatively cheap RuCl3.xH(2)O as a ligand-free catalyst. This readily available catalyst tolerates various amines comprising electron-deficient and electron-donating groups and allows them to transform into corresponding N-methylated products in moderate to excellent yields. In addition, few marketed pharmaceutical agents (e. g., venlafaxine and imipramine) were also successfully synthesized via late-stage functionalization from readily available feedstock chemicals, highlighting synthetic value of this advanced N-methylation reaction. Using this platform, we also attempted tandem reactions with selected nitroarenes to convert them into corresponding N-methylated amines using MeOH under H-2-free conditions including transfer hydrogenation of nitroarenes-to-anilines and prepared drug molecules (e. g., benzocaine and butamben) as well as key pharmaceutical intermediates. We further enable one-shot selective and green syntheses of 1-methylbenzimidazole using ortho-phenylenediamine (OPDA) and methanol as coupling partners.

Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Sarki, N; Goyal, V; Tyagi, NK; Puttaswamy; Narani, A; Ray, A; Natte, K or concate me.

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

Chemistry Milestones Of 100-19-6

Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Swamy, PCA; Varenikov, A; de Ruiter, G or concate me.

An article Direct Asymmetric Hydrogenation and Dynamic Kinetic Resolution of Aryl Ketones Catalyzed by an Iridium-NHC Exhibiting High Enantio- and Diastereoselectivity WOS:000510786100001 published article about N-HETEROCYCLIC CARBENES; STEREODIRECTING LIGANDS; STEREOSELECTIVE HYDROGENATION; RHODIUM COMPLEXES; HYDROSILYLATION; ALKENES; BEARING in [Swamy, Chinna Ayya P.; Varenikov, Andrii; de Ruiter, Graham] Technion Israel Inst Technol, Schulich Fac Chem, IL-3200008 Haifa, Israel in 2020.0, Cited 67.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A chiral iridium carbene-oxazoline catalyst is reported that is able to directly and efficiently hydrogenate a wide variety of ketones in excellent yields and good enantioselectivity (up to 93 % ee). Moreover, when using racemic alpha-substituted ketones, excellent diastereoselectivities were obtained (dr 99:1) by dynamic kinetic resolution of the in situ formed enolate. Overall, the herein described hydrogenation occurs under ambient conditions using low hydrogen pressures, providing a direct and atom efficient method towards chiral secondary alcohols.

Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Swamy, PCA; Varenikov, A; de Ruiter, G or concate me.

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