Machine Learning in Chemistry about 100-19-6

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

Authors Swamy, PCA; Varenikov, A; de Ruiter, G in AMER CHEMICAL SOC published article about N-HETEROCYCLIC CARBENES; RHODIUM COMPLEXES; ASYMMETRIC HYDROSILYLATION; STEREODIRECTING LIGANDS; PALLADIUM COMPLEXES; CARBONYL-COMPOUNDS; OLEFIN METATHESIS; ARYL-ALKYL; CATALYSTS; EFFICIENT 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 72.0. 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 report the synthesis and application of a versatile class of N-heterocyclic carbene ligands based on an imidazo[1,5-a]pyridine-3-ylidine backbone that is fused to a chiral oxazoline auxiliary. The key step in the synthesis of these ligands involves the installation of the oxazoline functionality via a microwave-assisted condensation of a cyano-azolium salt with a wide variety of 2-amino alcohols. The resulting chiral bidentate NHC-oxazoline ligands form stable complexes with rhodium(I) that are efficient catalysts for the enantioselective hydrosilylation of structurally diverse ketones. The corresponding secondary alcohols are isolated in good yields (typically >90%) with good to excellent enantioselectivities (80-93% ee). The reported hydrosilylation occurs at ambient temperatures (40 degrees C), with excellent functional group tolerability. Even ketones bearing heterocyclic substituents (e.g., pyridine or thiophene) or complex organic architectures are hydrosilylated efficiently, which is discussed further in this report.

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. 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

How did you first get involved in researching C8H7NO3

Quality Control of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Doherty, S; Knight, JG; Alshaikh, H; Wilson, J; Waddell, PG; Wills, C; Dixon, CM or send Email.

Quality Control of 1-(4-Nitrophenyl)ethanone. In 2021.0 EUR J INORG CHEM published article about ENANTIOSELECTIVE TRANSFER HYDROGENATION; OPENING METATHESIS POLYMERIZATION; RUTHENIUM ALLENYLIDENE COMPLEXES; MESOPOROUS SILICA; HIGHLY EFFICIENT; STEREOSELECTIVE-SYNTHESIS; CARBONYL-COMPOUNDS; RU CATALYST; POLYSTYRENE; ALCOHOLS in [Doherty, Simon; Knight, Julian G.; Wilson, James; Waddell, Paul G.; Wills, Corinne; Dixon, Casey M.] Newcastle Univ, Ctr Catalysis NUCAT, Sch Chem, Bedson Bldg, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England; [Alshaikh, Hind] King Abdulaziz Univ, Sci & Arts Coll, Dept Chem, Rabigh Campus, Jeddah 21911, Saudi Arabia in 2021.0, Cited 127.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The Noyori-Ikariya (arene)Ru(II)/TsDPEN precatalyst has been anchored to amorphous silica and DAVISIL through the eta(6)-coordinated arene ligand via a straightforward synthesis and the derived systems, (arene)Ru(II)/TsDPEN@silica and (arene)Ru(II)/TsDPEN@DAVISIL, form highly efficient catalysts for the asymmetric transfer hydrogenation of a range of electron-rich and electron-poor aromatic ketones, giving good conversion and excellent ee’s under mild reaction conditions. Moreover, catalyst generated in situ immediately prior to addition of substrate and hydrogen donor, by reaction of silica-supported [(arene)RuCl2](2) with (S,S)-TsDPEN, was as efficient as that generated from its preformed counterpart [(arene)Ru{(S,S)-TsDPEN}Cl]@silica. Gratifyingly, the initial TOFs (up to 1085 h(-1)) and ee’s (96-97 %) obtained with these catalysts either rivalled or outperformed those previously reported for catalysts supported by either silica or polymer immobilized through one of the nitrogen atoms of TsDPEN. While the high ee’s were also maintained during recycle studies, the conversion dropped steadily over the first three runs due to gradual leaching of the ruthenium.

Quality Control of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Doherty, S; Knight, JG; Alshaikh, H; Wilson, J; Waddell, PG; Wills, C; Dixon, CM or send Email.

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

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

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.. Recommanded Product: 1-(4-Nitrophenyl)ethanone

Recently I am researching about C-H ACTIVATION; 3+2 ANNULATION; CATALYZED SYNTHESIS; ACCESS; KETIMINES; FUNCTIONALIZATION; CYCLIZATION; VERSATILE; SYNTHONS; INDOLES, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21425415, 21774056]; National Basic Research Program of ChinaNational Basic Research Program of China [2015CB856303]; Science and Technology Department of Jiangsu Province [BRA2017360, BK20181255]. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Liu, ZS; Zhang, WJ; Guo, S; Zhu, J. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone. Recommanded Product: 1-(4-Nitrophenyl)ethanone

Transition-metal-catalyzed C-H activation synthesis of heterocyclic spiro[4,4]nonanes has persistently witnessed the use of additional stoichiometric transition-metal oxidant when employing C=C bond as the Spiro ring closure site. Herein, we have addressed the issue by reporting a redox-neutral strategy for spiro[indene-1,4′-oxa-zolidinones] synthesis via Rh(III)-catalyzed coupling of 4-phenyl-1,3-oxazol-2(3H)-ones with alkynes. The synthesis features a broad substrate scope and high regiospecificity.

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

Extracurricular laboratory: Synthetic route of 100-19-6

Safety of 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.

Sanad, SMH; Mekky, AEM in [Sanad, Sherif M. H.; Mekky, Ahmed E. M.] Cairo Univ, Fac Sci, Chem Dept, Giza 12613, Egypt published Synthesis, cytotoxicity and in vitro antibacterial screening of novel hydrazones bearing thienopyridine moiety as potent COX-2 inhibitors in 2020.0, Cited 58.0. 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.

The starting precursors 2-carbohydrazides, bearing thienopyridine moiety, were prepared using 2-thioxopyridine-3-carbonitriles as key synthons. Next, 2-carbohydrazides were reacted with a variety of 4-substituted benzylidinemalononitriles or 4-substituted benzaldehydes to afford a new series of the target hydrazones incorporating thienopyridine moiety. The elemental analyses and spectral data were used to demonstrate the structures of new hydrazones series. The in vitro antibacterial activities of the target hydrazones were evaluated against different strains of Gram-positive and Gram-negative bacteria. In comparison with chloramphenicol as a reference drug, hydrazones 13b, 13c and 13d, linked to p-C1, p-Br and p-Me moiety, respectively, exhibited the strongest activities against all tested bacteria with MIC values in the range of 6.2-12.5 mu g/mL. In addition, several new hydrazones were tested as in vitro cytotoxic agents against each of human breast carcinoma MCF-7 cell line, colon cancer Caco2 cell line and liver hepatocellular carcinoma HEPG2 cell line. The hydrazones 13b, 13c and 13d demonstrated the best cytotoxicity against the tested eukaryotic cells. Furthermore, both experimental and docking studies could predict the promising inhibitory activities of hydrazones 13c and 13d against COX-2 enzyme with IC 50 of 0.110 and 0.104 mu M, respectively, when compared with Celecoxib (IC50 of 0.115 mu M). [GRAPHICS] .

Safety of 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

Now Is The Time For You To Know The Truth About 100-19-6

Welcome to talk about 100-19-6, If you have any questions, you can contact Rammurthy, B; Peraka, S; Vasu, A; Sai, GK; Rohini, YD; Narender, N or send Email.. COA of Formula: C8H7NO3

Authors Rammurthy, B; Peraka, S; Vasu, A; Sai, GK; Rohini, YD; Narender, N in WILEY-V C H VERLAG GMBH published article about BAEYER-VILLIGER OXIDATION; RETRO-CLAISEN CONDENSATION; C-NUCLEOSIDE SYNTHESIS; CARBON-CYANO; DIRECT CONVERSION; ORGANIC-ACIDS; HALLER-BAUER; CLEAVAGE; ESTERS; MILD in [Rammurthy, Banothu; Peraka, Swamy; Vasu, Amrutham; Sai, Gajula Krishna; Rohini, Yennamaneni Divya; Narender, Nama] Acad Sci & Innovat Res, CSIR HRDG Campus,Sect 19, Ghaziabad 201002, UP, India; [Rammurthy, Banothu; Peraka, Swamy; Vasu, Amrutham; Sai, Gajula Krishna; Rohini, Yennamaneni Divya; Narender, Nama] CSIR Indian Inst Chem Technol, C&FC Div, Hyderabad 500007, Telangana, India in 2021, Cited 88. COA of Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A novel metal-free catalytic one-pot approach has been developed for the esterification of aralkyl ketones with alcohols under open-air atmospheric conditions. The inexpensive iodide/oxone reagent system allowed the cascade C(sp(3))-H bond oxygenation, selective C-C bond cleavage and esterification through the both radical and ionic pathways in a stepwise manner in one-pot. This mild, convenient and economically viable catalytic method tolerates the various functional groups to provide the corresponding alkyl benzoates in up to 98% yields with up to 99% selectivity. The efficiency and feasibility of scale-up of the present catalytic system was demonstrated with gram scale experiments (up to 10 gram scale).

Welcome to talk about 100-19-6, If you have any questions, you can contact Rammurthy, B; Peraka, S; Vasu, A; Sai, GK; Rohini, YD; Narender, N or send Email.. COA of Formula: C8H7NO3

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

More research is needed about C8H7NO3

Application In Synthesis of 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.

Recently I am researching about DERIVATIVES, Saw an article supported by the . Published in SPRINGER in NEW YORK ,Authors: Gurevich, KG; Urakov, AL; Klen, EE; Samorodov, AV; Nikitina, IL; Khaliullin, FA; Nebogatova, VA; Makarova, NN; Shepilova, SO; Bashirova, LI; Khalimov, AR. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone. Application In Synthesis of 1-(4-Nitrophenyl)ethanone

Ethyl 2-[8-Arylmethylidenehydrazino-3-methyl-7-(1-oxothietan-3-yl)xanth-1-yl]acetates (IV) were synthesized via reactions of ethyl 2-[8-hydrazino-3-methyl-7-(1-oxothietan-3-yl)xanth-1-yl]acetic acid (III) with various benzaldehydes and acetophenones. The structures of the compounds were elucidated using IR and NMR spectroscopy and elemental analysis. The antiplatelet, anticoagulation, antioxidant, and anti-inflammatory activities were assessedin vitroand in laboratory animals to identify promising compounds exhibiting antiplatelet (hydrazoneIVd) and antioxidant properties (hydrazoneIVb). BothIVbandIVdaccording toin silicocalculations were characterized by the absence of toxic risks (mutagenicity, oncogenicity, reproductive toxicity, local irritation) and had acceptable topological polar surface area so that they were promising.

Application In Synthesis of 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

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

Welcome to talk about 100-19-6, If you have any questions, you can contact Zhou, WY; Lu, WMZ; Wang, H; Xia, ZZ; Zhai, SY; Zhang, Z; Ma, YJ; He, MY; Chen, Q or send Email.. Safety of 1-(4-Nitrophenyl)ethanone

Safety of 1-(4-Nitrophenyl)ethanone. Recently I am researching about LAYERED DOUBLE HYDROXIDE; OXIDATIVE MANNICH REACTION; MIXED-METAL OXIDES; TERTIARY-AMINES; HIGHLY EFFICIENT; H FUNCTIONALIZATION; CARBONYL-COMPOUNDS; HYDROGEN-PEROXIDE; AEROBIC OXIDATION; ACTIVE CATALYSTS, Saw an article supported by the Advanced Catalysis and Green Manufacturing Collaborative Innovation Center of Changzhou University; Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD); Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology [BM2012110]; Postgraduate Research &Practice Innovation Program of Jiangsu Province [KYCX19_1746]; Qinglan Project of Jiangsu Province; Natural Science Foundation of Jiangsu Province of ChinaNatural Science Foundation of Jiangsu Province [BK20181461]. Published in ELSEVIER in AMSTERDAM ,Authors: Zhou, WY; Lu, WMZ; Wang, H; Xia, ZZ; Zhai, SY; Zhang, Z; Ma, YJ; He, MY; Chen, Q. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

CuMgAl layered double hydroxide compounds (CuMgAl-LDHs) have been synthesized, characterized and in-vestigated in the aerobic CDC reactions. The results indicated that NH3 center dot H2O coprecipitated CuMgAl LDH (N-CuMgAl-LDH) was able to efficiently accelerate the CDC reactions between the alpha-Csp(3)-H of N-aryltetrahy-droisoquinolines and nucleophiles. A wide scope of N-aryltetrahydroisoquinoline analogues and nucleophiles with different C-H bonds (C-sp3-H, C-sp2-H and Csp-H) could be tolerated by the N-CuMgAl-LDH system. Compared with the sample using Na2CO3 as the precipitant (C-CuMgAl-LDH), N-CuMgAl-LDH showed higher catalytic activity, which probably was due to its higher surface acidity. Dual function of redox and acidity for the N-CuMgAl-LDH catalyst has been observed in the CDC reaction. According to the obtained catalytic results, kinetic isotope effect experiment and XPS analysis, iminium ion was proposed as the key intermediate, made possible by the cycle of Cu2+ and Cu+ under the aerobic conditions.

Welcome to talk about 100-19-6, If you have any questions, you can contact Zhou, WY; Lu, WMZ; Wang, H; Xia, ZZ; Zhai, SY; Zhang, Z; Ma, YJ; He, MY; Chen, Q or send Email.. Safety of 1-(4-Nitrophenyl)ethanone

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

Discovery of 100-19-6

Recommanded Product: 100-19-6. Welcome to talk about 100-19-6, 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 send Email.

In 2019.0 CHEMISTRYSELECT published article about ENANTIOSELECTIVE REDUCTION; MERRIFIELD; RESINS; AMINES 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 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. Recommanded Product: 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.

Recommanded Product: 100-19-6. Welcome to talk about 100-19-6, 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 send Email.

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

Chemical Properties and Facts of C8H7NO3

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.. Computed Properties of C8H7NO3

An article Discovery of Membrane-Bound Pyrophosphatase Inhibitors Derived from an Isoxazole Fragment WOS:000526402700030 published article about TRYPANOSOMA-BRUCEI; PUMPING PYROPHOSPHATASES; ACIDOCALCISOMES; BISPHOSPHONATES; TARGET in [Vidilaseris, Keni; Goldman, Adrian] Univ Helsinki, Div Biochem, Dept Biosci, FI-00014 Helsinki, Finland; [Goldman, Adrian] Univ Leeds, Sch Biomed Sci, Leeds LS2 9JT, W Yorkshire, England; [Goldman, Adrian] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England; [Johansson, Niklas G.; Turku, Ainoleena; Dreano, Loic; Perez, Daniel Ayuso; Zhang, Yuezhou; Tamminen, Matti; Grazhdankin, Evgeni; Kiriazis, Alexandros; af Gennas, Gustav Boije; Xhaard, Henri] Univ Helsinki, Drug Res Program, Div Pharmaceut Chem & Technol, Fac Pharm, FI-00014 Helsinki, Finland; [Khattab, Ayman; Meri, Seppo] Univ Helsinki, Malaria Res Lab, Translat Immunol Res Program, Dept Bacteriol & Immunol,Haartman Inst, FI-00014 Helsinki, Finland; [Wilkinson, Aaron; Fishwick, Colin W. G.] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England in 2020.0, Cited 34.0. Computed Properties of C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Membrane-bound pyrophosphatases (mPPases) regulate energy homeostasis in pathogenic protozoan parasites and lack human homologues, which makes them promising targets in e.g. malaria. Yet only few nonphosphorus inhibitors have been reported so far. Here, we explore an isoxazole fragment hit, leading to the discovery of small mPPase inhibitors with 6-10 mu M IC50 values in the Thermotoga maritima test system. Promisingly, the compounds retained activity against Plasmodium falciparum mPPase in membranes and inhibited parasite growth.

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.. Computed Properties of C8H7NO3

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

Chemical Research in 100-19-6

Welcome to talk about 100-19-6, If you have any questions, you can contact Zhang, ZY; Huang, ZZ; Pan, Y; Song, C or send Email.. Recommanded Product: 100-19-6

In 2020 HIGH PERFORM POLYM published article about GAS-TRANSPORT PROPERTIES; POLYIMIDES; MEMBRANES; POLYMERS in [Zhang, Zi-Yang; Huang, Zhen-Zhong; Pan, Yang; Song, Cheng] Jiangxi Normal Univ, Key Lab Funct Small Organ Mol, Minist Educ, Nanchang 330022, Jiangxi, Peoples R China in 2020, Cited 34. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 100-19-6

A new diamine bearing flexible ether, rigid pyridine, and bulky anthrone pendent group, 10,10-bis[4-(4-amino-2-pyridinoxy)phenyl]-9(10H)-anthrone (BAPPA), was prepared in three steps from anthrone. BAPPA was reacted with six conventional aromatic dianhydrides in N, N-dimethylacetamide (DMAc) to form the corresponding new poly(ether imide)s (PEIs) via the poly(ether amic acid) (PEAA) precursors with inherent viscosities ranging from 0.85 dL g(-1) to 1.26 dL g(-1) and thermal imidization. All the PEAAs could be cast from DMAc solution and thermally converted into transparent, flexible, and tough PEI films with tensile strength of 72.2-112.4 MPa, tensile modulus of 1.8-2.1 GPa, and elongation at break of 10-18%. These PEIs were predominantly amorphous and displayed excellent thermal stability with the glass transition temperature of 290-388 degrees C, the 5% weight loss temperature of 480-514 degrees C, and the residue of 68-43% at 800 degrees C in nitrogen. The PEIs derived from 1,4-bis(3,4-dicarboxyphenoxy)benzene dianhydride and 4,4 ‘-hexafluoroisopropylidenediphathalic anhydride exhibited excellent solubility in organic solvents such as N-methyl-2-pyrrolidinone, DMAc, N, N-dimethylformamide, pyridine, and even in tetrahydrofuran. Meanwhile, these PEIs also exhibited high optical transparency with the ultraviolet cutoff wavelength in the 374-427 nm range and the wavelength of 80% transparency in the range of 468-493 nm.

Welcome to talk about 100-19-6, If you have any questions, you can contact Zhang, ZY; Huang, ZZ; Pan, Y; Song, C or send Email.. Recommanded Product: 100-19-6

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