Month: November 2021

An article Nickel-Copper bimetallic mesoporous nanoparticles: As an efficient heterogeneous catalyst for N-alkylation of amines with alcohols WOS:000586013600001 published article about MCM-41 MOLECULAR-SIEVES; AROMATIC-AMINES; SILICA NANOPARTICLES; SOLVENT-FREE; OXIDATION; IRON; BENZYLATION; RUTHENIUM; AMINATION; SECONDARY in [Nasresfahani, Zahra; Kassaee, Mohamad Z.] Tarbiat Modares Univ, Dept Chem, POB 14155-175, Tehran, Iran in 2021, Cited 43. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. SDS of cas: 105-13-5

A bimetallic catalyst (Ni/Cu-MCM-41) is prepared via co-condensation method. The latter is characterized by Fourier transform infrared (FT-IR), X-ray powder diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), diffuse reflectance spectroscopy (DRS), and nitrogen adsorption-desorption analysis. Catalytic performance of Ni/Cu-MCM-41 is probed in N-alkylation of amines with alcohols through a hydrogen autotransfer process. Noteworthy, this catalytic system appears very efficient for synthesis of a range of secondary and tertiary amines in good to excellent isolated yields. Moreover, the catalyst is successfully recovered and reused four times without notable decrease in its activity.

SDS of cas: 105-13-5. Bye, fridends, I hope you can learn more about C8H10O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

An article Palladium-catalyzed one-pot synthesis of 2-substituted quinazolin-4(3H)-ones from o-nitrobenzamide and alcohols WOS:000640769800011 published article about CASCADE SYNTHESIS; QUINAZOLINONES; SYSTEM; 4(3H)-QUINAZOLINONES; 2-NITROBENZAMIDES; AMINOBENZAMIDES; CYCLIZATION; CHEMISTRY; EFFICIENT; STRATEGY in [Wang, Ke; Chen, Hao; Dai, Xinyan; Huang, Xupeng; Feng, Zhiqiang] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing Key Lab Act Subst Discovery & Drugabil Ev, 1 Xiannongtan St, Beijing 100050, Peoples R China in 2021, Cited 41. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. HPLC of Formula: C8H10O2

Palladium-catalyzed 2-substituted quinazolin-4(3H)-one formation from readily available o-nitrobenzamides and alcohols using hydrogen transfer is described. Various quinazolin-4(3H)-ones were obtained in good to high yields. The cascade reaction including alcohol oxidation, nitro reduction, condensation, and dehydrogenation occurs without any added reducing or oxidizing agent.

HPLC of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Wang, K; Chen, H; Dai, XY; Huang, XP; Feng, ZQ or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Computed Properties of C8H10O2. Wu, JJ; Darcel, C in [Wu, Jiajun; Darcel, Christophe] Univ Rennes, CNRS ISCR, Inst Sci Chim Rennes, UMR 6226, F-35000 Rennes, France published Iron-Catalyzed Hydrogen Transfer Reduction of Nitroarenes with Alcohols: Synthesis of Imines and Aza Heterocycles in 2021, Cited 137. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

A straightforward and selective reduction of nitroarenes with various alcohols was efficiently developed using an iron catalyst via a hydrogen transfer methodology. This protocol led specifically to imines in 30-91% yields, with a good functional group tolerance. Noticeably, starting from o-nitroaniline derivatives, in the presence of alcohols, benzimidazoles can be obtained in 64-72% yields when the reaction was performed with an additional oxidant, DDQ, and quinoxalines were prepared from 1,2-diols in 28-96% yields. This methodology, unprecedented at iron for imines, also provides a sustainable alternative for the preparation of quinoxalines and benzimidazoles.

Welcome to talk about 105-13-5, If you have any questions, you can contact Wu, JJ; Darcel, C or send Email.. Computed Properties of C8H10O2

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Computed Properties of C8H10O2. Authors Zhuang, XH; Shi, XY; Zhu, R; Sun, B; Su, WK; Jin, C in ROYAL SOC CHEMISTRY published article about in [Zhuang, Xiaohui; Sun, Bin; Su, WeiKe; Jin, Can] Zhejiang Univ Technol, Collaborat Innovat Ctr Yangtze River Delta Reg Gr, Hangzhou, Peoples R China; [Shi, Xiayue; Zhu, Rui; Su, WeiKe; Jin, Can] Zhejiang Univ Technol, Coll Pharmaceut Sci, Hangzhou, Peoples R China in 2021, Cited 58. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A mild and metal-free protocol for visible-light induced intramolecular radical cyclization of N-allyl(propargyl)-2-bromo-2,2-difluoro-N-arylacetamide has been developed. This strategy showed excellent regioselectivity and simple operation to synthesize 4-substituted 3,3-difluoro-gamma-lactams with a broad substrate scope. Moreover, mechanistic studies revealed that this transformation proceeded through a cascade radical-type cyclization and hydrogen atom transfer process with PMDETA as a hydrogen-atom donor.

Welcome to talk about 105-13-5, If you have any questions, you can contact Zhuang, XH; Shi, XY; Zhu, R; Sun, B; Su, WK; Jin, C or send Email.. Computed Properties of C8H10O2

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Safety of (4-Methoxyphenyl)methanol. In 2021 TETRAHEDRON LETT published article about TRANSITION-METAL-FREE; S BOND FORMATION; AMIDE SYNTHESIS; ONE-POT; AMINES; EFFICIENT; ALCOHOLS; ALPHA; NANOPARTICLES; PD in [Rerkrachaneekorn, Tanawat; Tankam, Theeranon; Sukwattanasinitt, Mongkol; Wacharasindhu, Sumrit] Chulalongkorn Univ, Fac Sci, Nanotec CU Ctr Excellence Food & Agr, Dept Chem, Bangkok 10330, Thailand; [Wacharasindhu, Sumrit] Chulalongkorn Univ, Fac Sci, Dept Chem, Green Chem Fine Chem Prod STAR, Bangkok 10330, Thailand in 2021, Cited 62. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

In this research, we have developed a mild electrochemical process for oxidative amidation of benzyl alcohols/aromatic aldehydes with cyclic amines into the corresponding benzamides. This electroorganic synthetic method proceeds using NaI as a redox mediator under ambient temperature in undivided cell, providing more than 25 examples of amide products in moderate to good yields. The benefits of this reaction include one-pot synthesis, open air condition, proceed in aqueous media and no requirement of external conducting salt, base and oxidant. (C) 2021 Elsevier Ltd. All rights reserved.

Safety of (4-Methoxyphenyl)methanol. Bye, fridends, I hope you can learn more about C8H10O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

HPLC of Formula: C8H10O2. Authors Cavallo, M; Arnodo, D; Mannu, A; Blangetti, M; Prandi, C; Baratta, W; Baldino, S in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Cavallo, Marzia; Arnodo, Davide; Mannu, Alberto; Blangetti, Marco; Prandi, Cristina; Baldino, Salvatore] Dipartimento Chim, Via P Giuria 7, I-10125 Turin, Italy; [Baratta, Walter] Univ Udine, Dipartimento DI4A, Via Cotonificio 108, I-33100 Udine, Italy in 2021, Cited 52. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

The employment of easily affordable ruthenium(II)-complexes as pre-catalysts in the transfer hydrogenation of carbonyl compounds in deep eutectic media is described for the first time. The eutectic mixture tetrabutylammonium bromide/formic acid = 1/1 (TBABr/HCOOH = 1/1) acts both as reaction medium and hydrogen source. The addition of a base is required for the process to occur. An extensive optimization of the reaction conditions has been carried out, in terms of catalyst loading, type of complexes, H-2-donors, reaction temperature and time. The combination of the dimeric complex [RuCl(p-cymene)-mu-Cl](2) (0.01-0.05 eq.) and the ligand dppf (1,10-ferrocenediyl-bis(diphenylphosphine)ferrocene) in 1/1 molar ratio has proven to be a suitable catalytic system for the reduction of several and diverse aldehydes and ketones to their corresponding alcohols under mild conditions (40-60 degrees C) in air, showing from moderate to excellent tolerability towards different functional groups (halogen, cyano, nitro, phenol). The reduction of imine compounds to their corresponding amine derivatives was also studied. In addition, the comparison between the results obtained in TBABr/HCOOH and in organic solvents suggests a non-innocent effect of the DES medium during the process. (C) 2021 Elsevier Ltd. All rights reserved.

HPLC of Formula: C8H10O2. Bye, fridends, I hope you can learn more about C8H10O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Donthireddy, SNR; Pandey, VK; Rit, A in [Donthireddy, S. N. R.; Pandey, Vipin K.; Rit, Arnab] Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India published [(PPh3)(2)NiCl2]-Catalyzed C-N Bond Formation Reaction via Borrowing Hydrogen Strategy: Access to Diverse Secondary Amines and Quinolines in 2021, Cited 57. Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Commercially available [(PPh3)(2)NiCl2] was found to be an efficient catalyst for the mono-N-alkylation of (hetero)aromatic amines, employing alcohols to deliver diverse secondary amines, including the drug intermediates chloropyramine (5b) and mepyramine (5c), in excellent yields (up to 97%) via the borrowing hydrogen strategy. This method shows a superior activity (TON up to 10000) with a broad substrate scope at a low catalyst loading of 1 mol % and a short reaction time. Further, this strategy is also successful in accessing various quinoline derivatives following the acceptorless dehydrogenation pathway.

Welcome to talk about 105-13-5, If you have any questions, you can contact Donthireddy, SNR; Pandey, VK; Rit, A or send Email.. Formula: C8H10O2

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Authors Luo, NH; Zhong, YH; Wen, HL; Shui, HL; Luo, RS in WILEY-V C H VERLAG GMBH published article about in [Luo, Nianhua; Zhong, Yuhong; Wen, Huiling; Shui, Hongling; Luo, Renshi] Gannan Med Univ, Sch Pharmaceut Sci, Ganzhou 341000, Jiangxi, Peoples R China in 2021, Cited 94. COA of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Ketones are of great importance in synthesis, biology, and pharmaceuticals. This paper reports an iridium complexes-catalyzed cross-coupling of alcohols via hydrogen borrowing, affording a series of alpha-alkylated ketones in high yield (86 %-95 %) and chemoselectivities (>99 : 1). This methodology has the advantages of low catalyst loading (0.1 mol%) and environmentally benign water as the solvent. Studies have shown the amount of base has a great impact on chemoselectivities. Meanwhile, deuteration experiments show water plays an important role in accelerating the reduction of the unsaturated ketones intermediates. Remarkably, a gram-scale experiment demonstrates this methodology of iridium-catalyzed cross-coupling of alcohols has potential application in the practical synthesis of alpha-alkylated ketones.

COA of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Luo, NH; Zhong, YH; Wen, HL; Shui, HL; Luo, RS or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Safety of (4-Methoxyphenyl)methanol. I found the field of Chemistry very interesting. Saw the article Palladium-catalyzed one-pot synthesis of 2-substituted quinazolin-4(3H)-ones from o-nitrobenzamide and alcohols published in 2021, Reprint Addresses Feng, ZQ (corresponding author), Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, Beijing Key Lab Act Subst Discovery & Drugabil Ev, 1 Xiannongtan St, Beijing 100050, Peoples R China.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol.

Palladium-catalyzed 2-substituted quinazolin-4(3H)-one formation from readily available o-nitrobenzamides and alcohols using hydrogen transfer is described. Various quinazolin-4(3H)-ones were obtained in good to high yields. The cascade reaction including alcohol oxidation, nitro reduction, condensation, and dehydrogenation occurs without any added reducing or oxidizing agent.

Safety of (4-Methoxyphenyl)methanol. Bye, fridends, I hope you can learn more about C8H10O2, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Recently I am researching about AEROBIC OXIDATION; SILICA; EPOXIDATION; TEMPO, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21776260, 21773211, 21773210]; (Ascletis Biopharmaceutical (Hangzhou) Co., Ltd). Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Tian, YW; Guo, XQ; Li, MC; Li, CM; Hu, XQ; Jin, LQ; Sun, N; Hu, BX; Shen, ZL. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol. HPLC of Formula: C8H10O2

Herein, we designed and synthesized an SBA-15 supported 1-methyl-2-azaadamanane N-oxyl (1-Me-AZADO) and investigated its catalytic performance for selective oxidation of alcohols under Anelli’s conditions. The first example of immobilization of 1-Me-AZADO was very important to advance the oxgenation effectively because this supported N-oxyl has excellent catalytic activity for oxidation of alcohols to carbonyl compounds, and more importantly, it can be conveniently recovered and reused at least 6 times without significant effect on its catalytic efficiency.

HPLC of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Tian, YW; Guo, XQ; Li, MC; Li, CM; Hu, XQ; Jin, LQ; Sun, N; Hu, BX; Shen, ZL or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts