Tag: M.W=150-200

Recommanded Product: 1-(4-Nitrophenyl)ethanone. In 2020.0 ASIAN J ORG CHEM published article about ALPHA-AMINO-ACIDS; CARBOLINE DERIVATIVES; GAMMA-CARBOLINE; TANDEM REACTION; INDOLE; AMINATION; STRATEGY in [Yang, Tang-Hao; Kavala, Veerababurao; Kuo, Chun-Wei; Yao, Ching-Fa] Natl Taiwan Normal Univ, Dept Chem, Taipei, Taiwan in 2020.0, Cited 39.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The present methodology describes a versatile pathway to furnish alpha-carbolines from relatively stable 2-amino indole derivatives and 3-bromopropenal. High substrate tolerance, nonmetallic, more efficient, and mild reaction conditions are important aspects.

Welcome to talk about 100-19-6, If you have any questions, you can contact Yang, TH; Kavala, V; Kuo, CW; Yao, CF or send Email.. Recommanded Product: 1-(4-Nitrophenyl)ethanone

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

An article Synthesis of Nitrile-Bearing Quaternary Centers by an Equilibrium-Driven Transnitrilation and Anion-Relay Strategy WOS:000476452700044 published article about REDUCTIVE DECYANATION; CATALYZED CYANATION; LITHIUM REAGENTS; METAL EXCHANGE; CHEMISTRY ARC; POTASSIUM; GRIGNARD; HYDROCYANATION; DERIVATIVES; ALKYLATIONS in [Alazet, Sebastien; West, Michael S.; Patel, Purvish; Rousseaux, Sophie A. L.] Univ Toronto, Dept Chem, Davenport Res Labs, 80 St George St, Toronto, ON M5S 3H6, Canada in 2019, Cited 53. The Name is 2,2-Diphenylacetonitrile. Through research, I have a further understanding and discovery of 86-29-3. Recommanded Product: 2,2-Diphenylacetonitrile

The efficient preparation of nitrile-containing building blocks is of interest due to their utility as synthetic intermediates and their prevalence in pharmaceuticals. As a result, significant efforts have been made to develop methods to access these motifs which rely on safer and non-toxic sources of CN. Herein, we report that 2-methyl-2-phenylpropanenitrile is an efficient, non-toxic, electrophilic CN source for the synthesis of nitrile-bearing quaternary centers by a thermodynamic transnitrilation and anion-relay strategy. This one-pot process leads to nitrile products resulting from the gem-difunctionalization of alkyl lithium reagents.

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.. Recommanded Product: 2,2-Diphenylacetonitrile

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

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. Du, YR; Xu, BH; Pan, JS; Wu, YW; Peng, XM; Wang, YF; Zhang, SJ in [Du, Yi-Ran; Xu, Bao-Hua; Pan, Jia-Sheng; Wang, Yao-Feng; Zhang, Suo-Jiang] Chinese Acad Sci, Beijing Key Lab Ion Liquids Clean Proc, CAS Key Lab Green Proc & Engn, State Key Lab Multiphase Complex Syst,Inst Proc E, Beijing 100190, Peoples R China; [Du, Yi-Ran; Xu, Bao-Hua; Zhang, Suo-Jiang] Univ Chinese Acad Sci, Sch Chem & Chem Engn, Beijing 100049, Peoples R China; [Pan, Jia-Sheng] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China; [Wu, Yi-Wei; Peng, Xiao-Ming] Beijing Inst Petrochem Technol, Beijing Key Lab Clean Fuel & Efficient Catalyt Re, Beijing 102617, Peoples R China published Confinement of Bronsted acidic ionic liquids into covalent organic frameworks as a catalyst for dehydrative formation of isosorbide from sorbitol in 2019.0, Cited 59.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

The confinement of Bronsted acidic 1-methyl-3-(3-sulfopropyl)-1H-imidazol-3-ium hydrosulfate ([PSMIm][HSO4]) into the channel walls of two-dimensional (2D) COFs using a one-pot self-assembly strategy was achieved by incorporating an imine-linked TPB-DMTP-COF (TPB, triphenylbenzene; DMTP, dimethoxyterephthaldehyde) as the host. An appropriate loading of [PSMIm][HSO4] is crucial for the BIL-COF hybrids to maintain proper geometry in the channel and sufficient acidic sites for the sorbitol substrate and sorbitan intermediate to enter and react. The best yield of isosorbide (97%) from sorbitol to date was obtained in the presence of BIL-COF-30 as the catalyst under optimized conditions. Besides, BIL-COF-30 can be recycled for at least five runs without activity loss.

Application In Synthesis of 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Du, YR; Xu, BH; Pan, JS; Wu, YW; Peng, XM; Wang, YF; Zhang, SJ or send Email.

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

Recently I am researching about ANTIMICROBIAL ACTIVITY; BIOLOGICAL EVALUATION; ACCURATE DOCKING; GLIDE; BENZIMIDAZOLE; DERIVATIVES; DESIGN, Saw an article supported by the UGCUniversity Grants Commission, India [F 18-1/2011 (BSR)]; UGC, New DelhiUniversity Grants Commission, India; Department of Science and Technology, New DelhiDepartment of Science & Technology (India) [DST-FIST-SR/FST/CSI-212/2010]. Published in SPRINGER in DORDRECHT ,Authors: Desai, NC; Vaja, DV; Joshi, SB; Khedkar, VM. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone. SDS of cas: 100-19-6

We have developed a simple synthetic protocol for the preparation of novel 3-(3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)-5-arylisoxazoles. The structure of synthesized compounds was elucidated by spectral techniques like FT-IR,H-1-NMR,C-13-NMR, and mass. The novel bioactive compounds3a-twere evaluated for in vitro antibacterial activity on several bacterial species. Compounds3c(-4-NO2),3o(-4-F), and3r(-3,4-Cl-2) exhibited good in vitro antibacterial activity. Furthermore, molecular docking on DNA gyrase subunit bcould shed some light on the mechanism of action which can serve as a guide for lead optimization. Graphic abstract

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

Authors Guirado, A; Vera, M; Martiz, B; Rodenas, F; Sandoval, JA; Alarcon, E; Bautista, D in GEORG THIEME VERLAG KG published article about ONE-POT SYNTHESIS; BIOLOGICAL EVALUATION; TAUTOMERIC STRUCTURE; EFFICIENT SYNTHESIS; FACILE SYNTHESIS; DERIVATIVES; 2,3-DIHYDRO-1H-IMIDAZO<1,2-B>PYRAZOL-2-ONES; 1-ARYL-4,4-DICHLOROBUT-3-EN-1-ONES; REDUCTION; PYRAZOLES in [Guirado, Antonio; Vera, Maria; Martiz, Bruno; Rodenas, Francisco; Sandoval, Jose A.; Alarcon, Enrique; Bautista, Delia] Univ Murcia, Fac Quim, Dept Quim Organ, Campus Espinardo, Murcia 30071, Spain in 2020.0, Cited 57.0. 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 synthesis of previously unattainable 2,5-disubstituted 4,5-dihydroimidazo[1,5-b]pyrazol-6-ones has been developed. Electrochemical reductions of readily available 2,2,2-trichloroethylideneacetophenones were followed by reaction with hydrazine, leading to 3-aryl-5-dichloromethyl-2-pyrazolines. These were treated with isocyanates to obtain the corresponding aminocarbonyl derivatives, which were found to be able to form an otherwise almost inaccessible imidazo[1,5-b]pyrazole ring system via a one-step reaction involving internal condensation followed by hydrogen chloride elimination and aromatization. The molecular- structures of 2-(4-methylphenyl)-5-tosyl-4,5-dihydro-imidazo[1,5-b]pyrazol-6-one, 5-dichloromethyl-N-(4-chlorophenyl)-4,5-dihydro-3-p-tolylpyrazole-1-carboxamide, and 5-(4-bromophenyl)-2-p-tolyl-4,5-dihydroimidazo[1,5-b]pyrazol-6-one were determined by X-ray crystallographic analysis.

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

An article Na2S-promoted reduction of azides in water: synthesis of pyrazolopyridines in one pot and evaluation of antimicrobial activity WOS:000465614900012 published article about BIOLOGICAL EVALUATION; PRIMARY AMINES; EFFICIENT; DERIVATIVES; REAGENT; INHIBITORS; CONVERSION; DISCOVERY; DESIGN; ACID in [Kale, Ashok; Medishetti, Nagaraju; Atmakur, Krishnaiah] Indian Inst Chem Technol, CSIR, Fluoro & Agro Chem Dept, Hyderabad 500007, Telangana, India; [Kanugala, Sirisha; Kumar, Ganesh C.] Indian Inst Chem Technol, CSIR, Med Chem & Pharmacol Div, Hyderabad 500007, Telangana, India; [Kale, Ashok; Medishetti, Nagaraju; Kanugala, Sirisha; Atmakur, Krishnaiah] Indian Inst Chem Technol, AcSIR, Hyderabad 500007, Telangana, India in 2019.0, Cited 48.0. Computed Properties of C8H7NO3. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Reduction of various azides using Na2S has been accomplished in water, and, in situ, the resulting amines on reaction with various ketones lead to pyrazolo[3,4-b]pyridines in one pot. Thus, a number of new trifluoromethyl-substituted pyrazolo[3,4-b]pyridine compounds have been prepared and screened for antimicrobial activity against different Gram-positive and Gram-negative strains. A good number of compounds, 4a, 4b, 4d, 4f, 4i, 4k, 4l, 4m, 4r and 4s, were found to possess promising activity. Notably, Na2S on hydrolysis in water generates H2S and NaOH, which facilitate the reduction of azides followed by intramolecular cyclization leading to the title compounds. To the best of our knowledge, this is the first report of the synthesis of the title compounds in aqueous medium in a one-pot reaction.

Welcome to talk about 100-19-6, If you have any questions, you can contact Kale, A; Medishetti, N; Kanugala, S; Kumar, CG; Atmakur, K or send Email.. Computed Properties of C8H7NO3

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

Computed Properties of C8H7NO3. In 2019.0 ORG BIOMOL CHEM published article about BIOLOGICAL EVALUATION; PRIMARY AMINES; EFFICIENT; DERIVATIVES; REAGENT; INHIBITORS; CONVERSION; DISCOVERY; DESIGN; ACID in [Kale, Ashok; Medishetti, Nagaraju; Atmakur, Krishnaiah] Indian Inst Chem Technol, CSIR, Fluoro & Agro Chem Dept, Hyderabad 500007, Telangana, India; [Kanugala, Sirisha; Kumar, Ganesh C.] Indian Inst Chem Technol, CSIR, Med Chem & Pharmacol Div, Hyderabad 500007, Telangana, India; [Kale, Ashok; Medishetti, Nagaraju; Kanugala, Sirisha; Atmakur, Krishnaiah] Indian Inst Chem Technol, AcSIR, Hyderabad 500007, Telangana, India in 2019.0, Cited 48.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Reduction of various azides using Na2S has been accomplished in water, and, in situ, the resulting amines on reaction with various ketones lead to pyrazolo[3,4-b]pyridines in one pot. Thus, a number of new trifluoromethyl-substituted pyrazolo[3,4-b]pyridine compounds have been prepared and screened for antimicrobial activity against different Gram-positive and Gram-negative strains. A good number of compounds, 4a, 4b, 4d, 4f, 4i, 4k, 4l, 4m, 4r and 4s, were found to possess promising activity. Notably, Na2S on hydrolysis in water generates H2S and NaOH, which facilitate the reduction of azides followed by intramolecular cyclization leading to the title compounds. To the best of our knowledge, this is the first report of the synthesis of the title compounds in aqueous medium in a one-pot reaction.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Kale, A; Medishetti, N; Kanugala, S; Kumar, CG; Atmakur, K or concate me.

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

COA of Formula: C8H7NO3. In 2019.0 ASIAN J ORG CHEM published article about C-H FUNCTIONALIZATION; COPPER-CATALYZED THIOLATION; MULTICOMPONENT REACTIONS; REGIOSELECTIVE SULFENYLATION; 3-COMPONENT SYNTHESIS; COUPLING REACTION; DOMINO REACTIONS; FACILE SYNTHESIS; BOND FORMATION; SULFUR BOND in [Reddy, Raju Jannapu; Shankar, Angothu; Kumari, Arram Haritha] Osmania Univ, Univ Coll Sci, Dept Chem, Hyderabad 500007, Andhra Pradesh, India in 2019.0, Cited 118.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A metal-free sequential one-pot three-component protocol is described for the synthesis of C3-functionalized imidazo[1,2-a]pyridines. A successive construction of imidazo[1,2-a]pyridine followed by iodine-catalysed sulfenylation has been achieved in a one-pot operation from readily available alpha-bromomethyl ketones, 2-aminopyridines and thiosulfonates. An immense array of 3-sulfenylimidazo[1,2-a]pyridines were obtained in good to high yields. Also, the method extended for the synthesis of C3-halogenated imidazo[1,2-a]pyridines using sodium halides in the presence of K2S2O8. Notably, the reaction between alpha-bromomethyl ketones and 2-aminopyridines in the presence of K2S2O8 to yield 3-bromo-2-aryl-imidazo[1,2-a]pyridines, thus implies alpha-bromomethyl ketones also served as brominating agent. Overall, the present sequential one-pot protocol is straightforward, operationally simple, tolerates a broad range of functional groups, and is reliable for gram-scale experiments.

COA of Formula: C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Reddy, RJ; Shankar, A; Kumari, AH or concate me.

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

I found the field of Chemistry very interesting. Saw the article Unlocking the catalytic potential of tris(3,4,5-trifluorophenyl)borane with microwave irradiation published in 2019.0. COA of Formula: C8H7NO3, Reprint Addresses Melen, RL (corresponding author), Cardiff Univ, Sch Chem, Main Bldg,Pk Pl, Cardiff CF10 3AT, S Glam, Wales.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone

The catalytic activity of tris(3,4,5-trifluorophenyl)borane has been explored in the 1,2-hydroboration reactions of unsaturated sub-strates. Under conventional conditions, the borane was found to be active only in the hydroboration of aldehyde, ketone and imine substrates, with alkenes and alkynes not being reduced effectively. The use of microwave irradiation on the other hand has permitted alkenes and alkynes to be hydroborated in good 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.. COA of Formula: C8H7NO3

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

In 2019.0 CHEM-ASIAN J 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. COA of Formula: C8H7NO3

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.

COA 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