Month: December 2021

Product Details of 105-13-5. Rerkrachaneekorn, T; Tankam, T; Sukwattanasinitt, M; Wacharasindhu, S 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 published NaI-mediated oxidative amidation of benzyl alcohols/aromatic aldehydes to benzamides via electrochemical reaction 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.

Welcome to talk about 105-13-5, If you have any questions, you can contact Rerkrachaneekorn, T; Tankam, T; Sukwattanasinitt, M; Wacharasindhu, S or send Email.. Product Details of 105-13-5

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Authors Verma, A; Hazra, S; Dolui, P; Elias, AJ in WILEY-V C H VERLAG GMBH published article about CARBOXYLIC-ACID SALTS; SECONDARY ALCOHOLS; DEHYDROGENATIVE OXIDATION; DIRECT FUNCTIONALIZATION; CROSS-COUPLINGS; COMPLEX BEARING; N-ALKYLATION; PPM LEVELS; WATER; COBALT in [Verma, Ashutosh; Hazra, Susanta; Dolui, Pritam; Elias, Anil J.] Indian Inst Technol, Dept Chem, New Delhi 110016, India in 2021, Cited 118. Application In Synthesis of (4-Methoxyphenyl)methanol. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Herein, we report a simple, efficient, and sustainable method for the synthesis of alpha-alkylated ketones and quinolines using a hydrogen-borrowing strategy, which has emerged as a greener alternative in organic transformation reactions. Synthesis of a range of alpha-alkylated ketones and quinoline derivatives was achieved by using the water-soluble [Ru(8-AQ)Cl(p-cym.)]Cl-+(-) [Ru]-1 (AQ=aminoquinoline) catalyst with water as the reaction medium. By adopting this strategy, we have synthesized alpha-alkylated ketones and quinolines using ketones or secondary alcohols as starting materials and the primary alcohol as a green and naturally abundant alkylating agent.

Application In Synthesis of (4-Methoxyphenyl)methanol. Welcome to talk about 105-13-5, If you have any questions, you can contact Verma, A; Hazra, S; Dolui, P; Elias, AJ or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

In 2021 CATAL LETT published article about AEROBIC OXIDATION; AROMATIC DIAMINES; MULTICOMPONENT REACTIONS; SELECTIVE OXIDATION; COUPLING REACTIONS; SCHIFF-BASE; NANOCATALYST; NANOPARTICLES; HANTZSCH; COPPER in [Nasseri, Mohammad Ali; Rezazadeh, Zinat; Kazemnejadi, Milad; Allahresani, Ali] Univ Birjand, Dept Chem, Fac Sci, Birjand 97175615, Iran in 2021, Cited 73. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. HPLC of Formula: C8H10O2

An efficient magnetically recyclable bimetallic catalyst by anchoring copper and manganese complexes on the Fe(3)O(4)NPs was prepared and named as Fe3O4@Cu-Mn. It was founded as a powerful catalyst for the domino one-pot oxidative benzimidazole and Biginelli reactions from benzyl alcohols as a green protocol in the presence of air, under solvent-free and mild conditions. Fe3O4@Cu-Mn NPs were well characterized by FT-IR, XRD, FE-SEM, TEM, VSM, TGA, EDX, DLS, and ICP analyses. The optimum range of parameters such as time, temperature, amount of catalyst, and solvent were investigated for the domino one-pot benzimidazole and Biginelli reactions to find the optimum reaction conditions. The catalyst was compatible with a variety of benzyl alcohols, which provides favorable products with good to high yields for all of derivatives. Hot filtration and Hg poisoning tests from the nanocatalyst revealed the stability, low metal leaching and heterogeneous nature of the catalyst. To prove the synergistic and cooperative effect of the catalytic system, the various homologues of the catalyst were prepared and then applied to a model reaction separately. Finally, the catalyst could be filtered from the reaction mixture simply, and reused for five consecutive cycles with a minimum loss in catalytic activity and performance. Graphic A new magnetically recyclable Cu/Mn bimetallic catalyst has been developed for domino one-pot oxidation-condensation of benzimidazole and Biginelli reactions from alcohols.

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.. HPLC of Formula: C8H10O2

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

In 2021 CHEM-EUR J published article about ENANTIOSELECTIVE AMINOLYSIS; PHARMACOLOGICAL-ACTIVITY; PYRROLIDINE DERIVATIVES; CYCLOPEPTIDE ALKALOIDS; 2,3-EPOXY ALCOHOLS; AEROBIC OXIDATION; ANTIFUNGAL AGENT; STEREOCHEMISTRY; ENTRY in [Kuriyama, Yuse; Sasano, Yusuke; Hoshino, Yoshihiko; Uesugi, Shun-ichiro; Yamaichi, Aoto; Iwabuchi, Yoshiharu] Tohoku Univ, Dept Organ Chem, Grad Sch Pharmaceut Sci, Aoba Ku, 6-3 Aoba, Sendai, Miyagi 9808578, Japan in 2021, Cited 38. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Product Details of 105-13-5

Highly regioselective intramolecular aminolysis of 3,4-epoxy amines has been achieved. Key features of this reaction are (1) chemoselective activation of epoxides in the presence of unprotected aliphatic amines in the same molecules by a La(OTf)(3) catalyst and (2) excellent regioselectivity for anti-Baldwin 5-endo-tet cyclization. This reaction affords 3-hydroxy-2-alkylpyrrolidines stereospecifically in high yields. DFT calculations revealed that the regioselectivity might be attributed to distortion energies of epoxy amine substrates. The use of this reaction was demonstrated by the first enantioselective synthesis of an antispasmodic agent prifinium bromide.

Product Details of 105-13-5. Welcome to talk about 105-13-5, If you have any questions, you can contact Kuriyama, Y; Sasano, Y; Hoshino, Y; Uesugi, S; Yamaichi, A; Iwabuchi, Y or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Recommanded Product: (4-Methoxyphenyl)methanol. Authors Li, Y; Pan, CS; Wang, GL; Leng, Y; Jiang, PP; Dong, YM; Zhu, YF in ROYAL SOC CHEMISTRY published article about in [Li, Yan; Pan, Chengsi; Wang, Guangli; Leng, Yan; Jiang, Pingping; Dong, Yuming] Jiangnan Univ, Int Joint Res Ctr Photorespons Mol & Mat, Sch Chem & Mat Engn, Wuxi 214122, Jiangsu, Peoples R China; [Zhu, Yongfa] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China in 2021, Cited 46. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Until now, the effective photocatalytic oxidation of benzyl alcohol to benzaldehyde with high selectivity is still a great challenge. It is reported that the carrier separation rate is the key factor affecting the photocatalytic activity, and the formation of heterojunction is an effective solution to hinder electron-hole recombination. SnS with a narrow band gap has excellent light absorption performance, which covers the whole visible light region. After compounding with g-C3N4, the light utilization of the SnS/g-C3N4 photocatalyst is effectively improved. In addition, a Z-scheme heterojunction is formed between SnS and g-C3N4 due to the matched energy levels, which accelerates the separation of electrons and holes and improves the conversion of benzyl alcohol effectively. In this paper, the charge separation is accelerated to promote the reaction by the in situ construction of Z-scheme heterojunctions; the preparation method, reaction mechanism and energy level structure of the photocatalyst can play a certain guiding role in the organic conversion reaction.

Welcome to talk about 105-13-5, If you have any questions, you can contact Li, Y; Pan, CS; Wang, GL; Leng, Y; Jiang, PP; Dong, YM; Zhu, YF or send Email.. Recommanded Product: (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Formula: C8H10O2. Authors Feng, XY; Pi, YH; Song, Y; Xu, ZW; Li, Z; Lin, WB in AMER CHEMICAL SOC published article about in [Feng, Xuanyu; Pi, Yunhong; Song, Yang; Xu, Ziwan; Lin, Wenbin] Univ Chicago, Dept Chem, Chicago, IL 60637 USA; [Pi, Yunhong; Li, Zhong] South China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Peoples R China in 2021, Cited 63. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

We report here the construction of two metal-organic frameworks (MOFs), Zr-6-Cu/Fe-1 and Zr-6–Cu/Fe-2, by integrating earth-abundant cuprous photosensitizers (Cu-PSs) and Fe catalysts for photocatalytic aerobic oxidation. Site isolation and pore confinement stabilize both Cu-PSs and Fe catalysts, while the proximity between active centers facilitates electron and mass transfer. Upon visible light irradiation and using O-2 as the only oxidant, Zr-6-Cu/Fe-1 and Zr-6-Cu/ Fe-2 efficiently oxidize alcohols and benzylic compounds to afford corresponding carbonyl products with broad substrate scopes, high turnover numbers of up to 500 with a 9.4-fold enhancement over homogeneous analogues, and excellent recyclability in four consecutive runs. Control experiments, spectroscopic evidence, and computational studies revealed the photooxidation mechanism: oxidative quenching of [Cu-PS]* by O-2 affords [Cu-II-PS], which efficiently oxidizes Fe-III-OH to generate a hydroxyl radical for substrate oxidation. This work highlights the potential of MOFs in promoting earth-abundant metal-based photocatalysis.

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.. Formula: C8H10O2

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

In 2021 EUR J ORG CHEM published article about CATALYZED AEROBIC DEHYDROGENATION; BIOLOGICAL EVALUATION; MOLECULAR-OXYGEN; HECK REACTION; 2′-AMINOCHALCONES; EFFICIENT; FLAVANONES; INHIBITORS; CHEMISTRY; QUINOLONE in [Kim, Young Min; Yoo, Hyung-Seok; Son, Seung Hwan; Kim, Ga Yeong; Jang, Hyu Jeong; Kim, Dong Hwan; Kim, Nam-Jung] Kyung Hee Univ, Coll Pharm, 26 Kyungheedae Ro, Seoul 02447, South Korea; [Kim, Soo Dong; Park, Boyoung Y.; Kim, Nam-Jung] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, 26 Kyungheedae Ro, Seoul 02447, South Korea in 2021, Cited 36. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. COA of Formula: C8H10O2

2-Aryl-2,3-dihydroquinolin-4(1H)-ones have recently been identified as important structures with potent biological activities such as antitumor and antidiabetic effect. Herein, a total of 25 novel N-Tf 2-aryl-2,3-dihydroquinolin-4(1H)-ones were expediently synthesized via the oxidative aza-Michael cyclization of N-Tf-2 ‘-aminodihydrochalcones by ligand-free palladium(II) catalysis. This study presents a new synthetic approach to yield N-Tf 2-aryl-2,3-dihydroquinolin-4(1H)-ones, which can be easily transformed into pharmacologically interesting aza-flavanones and other N-heterocycles, such as quinolines and tetrahydroquinolines, in yields up to 84 %. This methodology has various advantages, which includes short reaction times under mild conditions and suitable functional group tolerance. Furthermore, a plausible mechanism was proposed and demonstrated by kinetic analysis.

COA 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

COA of Formula: C8H10O2. In 2021 AUST J CHEM published article about VITAMIN-E in [Shahnavaz, Zohreh; Zaharani, Lia; Khaligh, Nader Ghaffari; Johan, Mohd Rafie] Univ Malaya, Inst Postgrad Studies, Nanotechnol & Catalysis Res Ctr, 3rd Floor,Block A, Kuala Lumpur 50603, Malaysia; [Mihankhah, Taraneh] Iran Univ Sci & Technol, Sch Civil Engn, Dept Water & Environm Engn, Environm Res Lab, Tehran 16765163, Iran in 2021, Cited 35. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

A new ionic liquid was synthesised, and its chemical structure was elucidated by FT-IR, 1D NMR, 2D NMR, and mass analyses. Some physical properties, thermal behaviour, and thermal stability of this ionic liquid were investigated. The formation of a two-protonic acid salt namely 4,4′-trimethylene-N,N’-dipiperidinium sulfate instead of 4,4′-trimethylene-N,N’-dipiperidinium hydrogensulfate was evidenced by NMR analyses. The catalytic activity of this ionic liquid was demonstrated in the esterification reaction of n-butanol and glacial acetic acid under different conditions. The desired acetate was obtained in 62-88% yield without using a Dean-Stark apparatus under optimal conditions of 10 mol-% of the ionic liquid, an alcohol to glacial acetic acid mole ratio of 1.3 : 1.0, a temperature of 75-100 degrees C, and a reaction time of 4 h. alpha-Tocopherol (alpha-TCP), a highly efficient form of vitamin E, was also treated with glacial acetic acid in the presence of the ionic liquid, and O-acetyl-alpha-tocopherol (Ac-TCP) was obtained in 88.4% yield. The separation of esters was conducted during workup without the utilisation of high-cost column chromatography. The residue and ionic liquid were used in subsequent runs after the extraction of desired products. The ionic liquid exhibited high catalytic activity even after five runs with no significant change in its chemical structure and catalytic efficiency.

COA of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Shahnavaz, Z; Zaharani, L; Khaligh, NG; Mihankhah, T; Johan, MR or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Authors Yang, SN; Liu, XY; Lu, SJ; Li, Z; Zhang, YM; Yu, SN; Song, J; Ding, CF; Yang, HY in WILEY-V C H VERLAG GMBH published article about in [Yang, Shouning; Yu, Shaoning; Yang, Huayan] Ningbo Univ, Sch Mat Sci & Chem Engn, Inst Mass Spectrometry, Zhejiang Prov Key Lab Adv Mass Spectrometry & Mol, Ningbo 315211, Zhejiang, Peoples R China; [Zhang, Yanmin; Song, Jian] Henan Normal Univ, Sch Phys, Xinxiang 453007, Henan, Peoples R China; [Yang, Shouning; Liu, Xiaoyang; Lu, Sijia; Li, Zhuo; Yang, Huayan] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine, Key Lab Green Chem Media & React, Minist Educ,Sch Chem & Chem Engn, Xinxiang 453007, Henan, Peoples R China in 2021, Cited 65. SDS of cas: 105-13-5. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

The development of eco-friendly and low cost catalysts is challenging. Here, heterostructures of Bi2S3 quantum dots (QDs) doped onto ultrathin BiOCl nanosheets were synthesized by a facile hydrothermal method to exploit efficient photosensitizers with appropriate electronic states to enhance the transfer of electrons. The obtained Bi2S3-BiOCl showed highly efficient photocatalytic ability for selective oxidation of aromatic alcohols to aldehydes. More oxygen vacancies are formed on the exposed 001 facet of the ultrathin BiOCl, which can effectively trap electrons and form O-.(2)- radicals. The cooperation between the BiOCl and the Bi2S3 QDs effectively separates photogenerated electron-hole pairs at the heterointerface and facilitates the cooperative actions of O-.(2)- radicals and holes, which brings about a desirable photocatalytic eciency for the selective oxidation of aromatic alcohols. This work highlights the synergistic effect of semiconductor QDs and two-dimensional materials on selective conversion processes and provides a new design paradigm using noble metal-free heteromaterials with high photocatalytic activity. This opens new possibilities for photocatalyst design using heteromaterials with high photocatalytic activity.

Welcome to talk about 105-13-5, If you have any questions, you can contact Yang, SN; Liu, XY; Lu, SJ; Li, Z; Zhang, YM; Yu, SN; Song, J; Ding, CF; Yang, HY or send Email.. SDS of cas: 105-13-5

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

SDS of cas: 105-13-5. In 2021 CHEM COMMUN published article about CONJUGATED MICROPOROUS POLYMERS; AEROBIC OXIDATION; ORGANIC FRAMEWORKS; CATALYTIC-SYSTEM; SUPPORTED TEMPO; CORE-SHELL; SPHERES; DESIGN in [Shen, Yan-Ming; Xue, Yun; Yan, Mi; Mao, Hui-Ling; Cheng, Hu; Chen, Zhuo; Yu, Xiu-Jun; Zhuang, Jin-Liang] Guizhou Normal Univ, Key Lab Funct Mat Chem Guizhou Prov, Sch Chem & Mat Sci, 116 Baoshan Rd North, Guiyang 550001, Peoples R China; [Sui, Zhi-Wei] Natl Inst Metrol, Ctr Adv Measurement Sci, Beijing, Peoples R China; [Zhu, Shao-Bin; Zhuang, Jin-Liang] NanoFCM INC, Xiamen Pioneering Pk Overseas Chinese Scholars, Xiamen 361005, Peoples R China; [Yu, Xiu-Jun] Goethe Univ Frankfurt, Inst Inorgan & Analyt Chem, Max von Laue Str 7, D-60438 Frankfurt, Germany in 2021, Cited 34. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

A bottom-up approach was developed to prepare TEMPO radical decorated hollow aromatic frameworks (HPAF-TEMPO) by using TEMPO radical functionalized monomers and SiO2 nanospheres as templates. The accessible inner layer, high density of TEMPO sites, and hybrid micro-/mesopores of the HPAF-TEMPO enable the aerobic oxidation of a broad range of alcohols with high efficiency and excellent selectivity.

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