Heterocyclic Building Blocks-benzodioxan

Al-Romaizan, AN; Ahmed, NS; Elfeky, SM in [Al-Romaizan, Abeer N.; Ahmed, Nesreen S.; Elfeky, Sherin M.] King Abdulaziz Univ, Dept Chem, Fac Sci, Jeddah 21589, Saudi Arabia; [Ahmed, Nesreen S.] Natl Res Ctr, Pharmaceut & Drug Ind Res Div, Dept Therapeut Chem, El Buhouth St, Cairo 12622, Egypt; [Elfeky, Sherin M.] Mansoura Univ, Dept Organ Pharmaceut Chem, Fac Pharm, Mansoura 355516, Egypt published Design, Synthesis, and Biological Evaluation of Triazolyl- and Triazinyl-Quinazolinediones as Potential Antitumor Agents in 2019.0, Cited 27.0. HPLC of Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Novel 6(3-1H-1,2,4-triazol-1-yl)-3-phenylquinazoline-2,4(1H,3H)-diones (7a-e) were synthesized from different enaminones (6a-e) with 6-hydrazinyl-3-phenylquinazoline-2,4(1H,3H)-dione. 2,6(4-2-Substituted-1,3,5-triazin-1(2H)-yl)-3-phenylquinazoline-2,4(1H,3H)-diones (8a-k) were synthesized from the reaction of 1-(2,4-dioxo-3-phenyl-1,2,3,4-tetrahydroquinazolin-6-yl)thiourea, urea, or guanidine (3a-c) with enaminones (6a-e), and a series from 3-substituted-2-imino-1,3,5-triazin-1(2H)-yl-sulfonyl-phenyl-1-methylquinazoline-2,4(1H,3H)-dione (12a-j) were obtained from the reaction of N-(diaminomethylene)-4-(1-methyl-2,4-dioxo-1,2-dihydroquinazolin-3(4H)-yl)benzenesulfonamide (11) with the enaminone (6a-j). The antitumor activity of the synthesized compounds was evaluated against two human cell lines: human colon carcinoma HCT116 and human hepatocellular carcinoma HEP-G2. Some of the tested compounds showed significant potency compared to the reference drug staurosporin.

HPLC of Formula: 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.

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

In 2020 ORGANOMETALLICS published article about ORGANOMETALLIC CHEMISTRY; COORDINATION CHEMISTRY; BOND-CLEAVAGE; NITRIC-OXIDE; LIGANDS; PNP; APPROXIMATION; HYDROBORATION; PLATINUM; IRIDIUM in [Pecak, Jan; Eder, Wolfgang; Linert, Wolfgang; Kirchner, Karl] Vienna Univ Technol, Inst Appl Synthet Chem, A-1060 Vienna, Austria; [Stoeger, Berthold] Vienna Univ Technol, Xray Ctr, A-1060 Vienna, Austria; [Realista, Sara] Univ Nova Lisboa, ITQB NOVA, Inst Tecnol Quim & Biol Antonio Xavier, P-2780157 Oeiras, Portugal; [Martinho, Paulo N.; Calhorda, Maria Jose] Univ Lisbon, Fac Ciencias, BioISI Biosyst & Integrat Sci Inst, DQB, P-1749016 Lisbon, Portugal in 2020, Cited 53. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3. Product Details of 86-29-3

The reaction of coordinatively unsaturated Co(II) PCP pincer complexes with nitric oxide leads to the formation of new, air-stable, diamagnetic mono nitrosyl compounds. The synthesis and characterization of five- and four-coordinate Co(III) and Co(I) nitrosyl pincer complexes based on three different ligand scaffolds is described. Passing NO through a solution of [Co(PCPNMe-iPr)Cl], [Co(PCPO-iPr)Cl] or [Co(PCPCH2-iPr)Br] led to the formation of the low-spin complex [Co(PCP-iPr)(NO)-X] with a strongly bent NO ligand. Treatment of the latter species with (X = CI, Br) AgBF4 led to chloride abstraction and formation of cationic square-planar Co(I) complexes of the type [Co(PCP-iPr)(NO)](+) featuring a linear NO group. This reaction could be viewed as a formal two electron reduction of the metal center by the NO radical from Co(III) to Co(I), if NO is counted as NO+. Hence, these systems can be described as {CoNO}(8) according to the Enemark-Feltham convention. X-ray structures, spectroscopic and electrochemical data of all nitrosyl complexes are presented. Preliminary studies show that [Co(PCPNMe-iPr)(NO)](+) catalyzes efficiently the reductive hydroboration of nitriles with pinacolborane (HBpin) forming an intermediate {CoNO}(8) hydride species.

Product Details of 86-29-3. Bye, fridends, I hope you can learn more about C14H11N, If you have any questions, you can browse other blog as well. See you lster.

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

Yu, YQ; Wu, QL; Liu, D; Hu, L; Yu, L; Tan, Z; Zhu, GG in [Yu, Yongqi; Wu, Qianlong; Liu, Da; Hu, Liang; Yu, Lin; Tan, Ze] Hunan Univ, Coll Chem & Chem Engn, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China; [Zhu, Gangguo] Zhejiang Normal Univ, Dept Chem, 688 Yingbin Rd, Jinhua 321004, Zhejiang, Peoples R China published Synthesis of Benzofulvenes via Cp*Co(III)-Catalyzed C-H Activation and Carbocyclization of Aromatic Ketones with Internal Alkynes in 2019.0, Cited 84.0. 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.

A highly efficient and practical synthesis of benzofulvenes was developed via ketone-directed Cp*Co(III)-catalyzed sequential C-H activation, addition, cyclization, and dehydration cascade processes between simple aromatic ketones and alkynes. The reaction tolerates a variety of functional groups, and various benzofulvenes were efficiently synthesized in 42-92% yields.

Safety of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Yu, YQ; Wu, QL; Liu, D; Hu, L; Yu, L; Tan, Z; Zhu, GG or send Email.

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

An article Controllable Sulfur, Nitrogen Co-doped Porous Carbon for Ethylbenzene Oxidation: The Role of Nano-CaCO3 WOS:000470179400028 published article about METAL-FREE CATALYST; ORDERED MESOPOROUS CARBON; OXYGEN REDUCTION; SELECTIVE OXIDATION; ELECTROCATALYTIC ACTIVITY; GRAPHENE; EFFICIENT; NANOTUBES; DESULFURIZATION; TEMPERATURE in [Qin, Yutian; Guo, Haotian; Wang, Bowei; Li, Jiayi; Gao, Ruixiao; Qiu, Pengzhi; Sun, Mingming; Chen, Ligong] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China; [Wang, Bowei; Chen, Ligong] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300072, Peoples R China; [Wang, Bowei; Chen, Ligong] Tianjin Engn Res Ctr Funct Fine Chem, Tianjin 300072, Peoples R China in 2019.0, Cited 57.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Safety of 1-(4-Nitrophenyl)ethanone

Heteroatom-doped porous carbon materials have exhibited promising applications in various fields. In this work, sulfur, nitrogen co-doped carbon materials (SNCs) with abundant pore structure were prepared by pyrolysis of sulfur, nitrogen-containing porous organic polymers (POPs) mixed with nano-CaCO3 at high temperature. Among the resultant materials, SNC-Ca-850 possesses a relatively high level of doped heteroatoms and exhibits an excellent catalytic performance for the selective oxidation of benzylic C-H bonds. It is noteworthy that nano-CaCO3 increases the doped sulfur content in the synthesized carbon materials to a large extent and impacts the existence modes of sulfur. In addition, it enhances the porous structure and specific surface area of the resultant SNCs significantly. This work provides a viable strategy to promote the doping of sulfur into carbon materials during the pyrolysis process.

Safety of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Qin, YT; Guo, HT; Wang, BW; Li, JY; Gao, RX; Qiu, PZ; Sun, MM; Chen, LG or send Email.

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

Quality Control of 1-(4-Nitrophenyl)ethanone. In 2020.0 CHEMISTRYSELECT published article about AROMATIC NITRO-COMPOUNDS; PHOTOCATALYTIC REDUCTION; CHEMOSELECTIVE REDUCTION; SELECTIVE HYDROGENATION; SUPPORTED PLATINUM; MESOPOROUS SBA-15; ACTIVE CATALYST; NANOPARTICLES; EFFICIENT; COPPER in [Thennila, Muthukumar; Muthumanickam, Shenbagapushpam; Selvakumar, Kodirajan] Thiagarajar Coll, Dept Chem Res, Madurai 625009, Tamil Nadu, India; [Thennila, Muthukumar; Sivabharathy, Madasamy] Sethu Inst Technol, Dept Phys, Virudunagar 626115, Tamil Nadu, India; [Yuvaraj, Paneerselvam] CSIR, North East Inst Sci & Technol, Branch Lab, Imphal 795004, Manipur, India in 2020.0, Cited 70.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A strategy for heterogeneous copper(I) mesoporous silica [Cu(I)-SBA-15] mediated catalytic reduction has been developed for the reduction of various nitroarenes in excellent yields. In addition to alcothermal strategy, other strategies have been attempted for the preparation of Cu(I) substituted mesoporous silica, however, the desired oxidation state is obtained only through alcothermal strategy. The crystalline phases and oxidation state of synthesized materials were characterized by XRD and XPS measurements and tested for catalytic reduction of nitroarenes. Among the tested materials, the best catalytic reduction of nitroarenes with an excellent substrate scope and good catalytic reusability was established by Cu(I)-SBA-15 material. The reduction kinetics and the controlled experimental studies reveal that the reaction proceeds through pseudo-first-order kinetics and nitrosobenzene intermediate pathway.

Quality Control of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Thennila, M; Muthumanickam, S; Sivabharathy, M; Yuvaraj, P; Selvakumar, K or send Email.

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

An article Novel 2,6-diketopiperazine-derived acetohydroxamic acids as promising anti-Trypanosoma brucei agents WOS:000482296400004 published article about DESIGN in [Fytas, George; Zoidis, Grigoris; Tsatsaroni, Alexandra; Tsotinis, Andrew] Univ Athens, Dept Pharmaceut Chem, Fac Pharm, Sch Hlth Sci, GR-15771 Athens, Greece; [Taylor, Martin C.; Kelly, John M.] London Sch Hyg & Trop Med, Dept Pathogen Mol Biol, Keppel St, London WC1E 7HT, England in 2019.0, Cited 15.0. Category: benzodioxans. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Aim: Identification of new, effective and selective trypanocidal agents. Materials & methods: Twelve novel acetohydroxamic acid derivatives based on 2-alkyl-2-aryl-2,6-diketopiperazine scaffolds have been synthesized and evaluated in vitro for their growth inhibitory activity against bloodstream form Trypanosoma brucei. Results: All the analogs were remarkably potent inhibitors, with low micromolar to submicromolar activities. Structure-activity relationship studies demonstrated that the presence of an alkyl substituent at the N(4)-position of the 2,6-diketopiperazine ring portion was, in general, beneficial to trypanocidal activity in this series. Conclusion: The highest activity resulted from the introduction of a methyl, n-propyl or n-butyl substituent to the N(4)-position of the parent compound. Importantly, the most potent analogs were found to be highly selective against T brucei with respect to mammalian cells. [GRAPHICS] .

Category: benzodioxans. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Fytas, G; Zoidis, G; Taylor, MC; Kelly, JM; Tsatsaroni, A; Tsotinis, A or concate me.

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

An article Synthesis, Stability, and (De)hydrogenation Catalysis by Normal and Abnormal Alkene- and Picolyl-Tethered NHC Ruthenium Complexes WOS:000474812100005 published article about N-HETEROCYCLIC CARBENES; IRIDIUM COMPLEXES; COORDINATION; ACTIVATION; LIGANDS; REMOTE; RU; IMIDAZOLIUM; OXIDATION; BEHAVIOR in [Malan, Frederick P.; Singleton, Eric; van Rooyen, Petrus H.; Landman, Marile] Univ Pretoria, Dept Chem, 02 Lynnwood Rd, ZA-0002 Pretoria, South Africa; [Albrecht, Martin] Univ Bern, Dept Chem & Biochem, Freiestr 3, CH-3012 Bern, Switzerland 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. Name: 1-(4-Nitrophenyl)ethanone

A series of p-cymene and cyclopentadienyl Ru(II)-aNHC complexes were synthesized from 2-methylimidazolium salts with either an N-bound alkenyl (1, 3) or picolyl tether (6, 7). The C(5)-Me substituted alkenyl-tethered analogues (2, 4) were also synthesized. Ag-mediated C(2)-dealkylation was a prominent side reaction that led to the formation of normally bound NHC Ru(II) complexes, which in selected cases were isolated (5, 8). A C(4)- over C(2)-selectivity for ruthenium binding was established by protecting the C(2)-position with an iPr group on the imidazolium precursor, for which unique p-cymene (9) and cyclopentadienyl (10) Ru(II)-aNHC derivatives were synthesized. All complexes were applied in the transfer hydrogenation of ketones and in secondary alcohol oxidation, with higher catalytic activity for the p-cymene over the cyclopentadienyl systems, as well as the alkenyl- over the picolyl-containing aNHC complexes.

Name: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Malan, FP; Singleton, E; van Rooyen, PH; Albrecht, M; Landman, M or send Email.

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

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. Name: 1-(4-Nitrophenyl)ethanone

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.. Name: 1-(4-Nitrophenyl)ethanone

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

I found the field of Chemistry very interesting. Saw the article Convenient One-Pot Synthesis of Allylsilanes from Enolizable Ketones published in 2019.0. SDS of cas: 100-19-6, Reprint Addresses Kwan, MLD (corresponding author), John Carroll Univ, Dept Chem, 1 John Carroll Blvd, University Hts, PA 44118 USA.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

A convenient one-pot synthesis of allylsilanes from enolizable methyl aryl ketones has been developed. The first step involves nucleophilic addition of the trimethylsilylmethyl group to ketones using the alkylation method developed by Ishihara with slight modification to generate the corresponding beta-silylalkoxides. The second step entails addition of diisobutylaluminum chloride and heating at about 130 degrees C overnight to afford allylsilanes in fair yields.

SDS of cas: 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.

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

An article Co-MOF-Derived Hierarchical Mesoporous Yolk-shell-structured Nanoreactor for the Catalytic Reduction of Nitroarenes with Hydrazine Hydrate WOS:000477986300022 published article about POROUS CARBON SHELL; DOPED CARBON; HYDROGENATION; EFFICIENT; NANOTUBES; NANOPARTICLES; PERFORMANCE; ULTRAFINE; AU; NANOSTRUCTURES in [Yuan, Man; Yang, Chen; Wang, Fanhao; Dong, Zhengping] Lanzhou Univ, Lab Special Funct Mat & Struct Design, Gansu Prov Engn Lab Chem Catalysis, Minist Educ,Coll Chem & Chem Engn, Lanzhou 730000, Gansu, Peoples R China; [Zhang, Hongbo] Lanzhou Univ, Sch Phys Sci & Technol, Inst Nanosci & Nanotechnol, Lanzhou 730000, Gansu, Peoples R China in 2019.0, Cited 67.0. Formula: C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Porous nanoreactors demonstrate immense potential for applications in heterogeneous catalysis due to their excellent mass-transfer performance and stability. The design of a simple, universal strategy for fabricating nanoreactor catalysts is of significance for organic transformation. In this study, a nanoreactor with a hierarchical mesoporous yolk-shell structure was successfully prepared by the high-temperature carbonization of a ZIF-67@polymer composite. The core of the resultant Co@ZDC@mC material comprised Co NPs anchored in the ZIF-67-derived carbon framework, while the shell comprised resin-polymer-derived mesoporous carbon. The as-obtained Co@ZDC@mC-700 catalyst enriched reactants, efficiently catalyzed the reaction in the core, and permitted the desorption of the product from the nanoreactor. In the catalytic reduction of nitrobenzene with N2H4.H2O, Co@ZDC@mC-700 exhibited superior catalytic efficiency (TOF=1136.3 h(-1)). In addition, Co@ZDC@mC-700 exhibited excellent performance for the catalytic reduction of various functionalized nitroarenes, as well as good reusability and recyclability. Hence, a simple, useful approach for fabricating a metal-organic-framework-derived non-noble metal-based yolk-shell nanoreactor for effective catalytic transformation is proposed.

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.. Formula: C8H7NO3

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