Category: 105-13-5

Safety of (4-Methoxyphenyl)methanol. Authors Alam, MN; Dash, SR; Mukherjee, A; Pandole, S; Marelli, UK; Vanka, K; Maity, P in AMER CHEMICAL SOC published article about in [Alam, Md Nirshad; Mukherjee, Anirban; Pandole, Satish; Marelli, Udaya Kiran; Maity, Pradip] CSIR Natl Chem Lab, Organ Chem Div, Pune 411008, Maharashtra, India; [Alam, Md Nirshad; Dash, Soumya Ranjan; Marelli, Udaya Kiran; Vanka, Kumar] Acad Sci & Innovat Res AcSIR, Ghaziabad 201002, India; [Dash, Soumya Ranjan; Vanka, Kumar] CSIR Natl Chem Lab, Phys & Mat Chem Div, Pune 411008, Maharashtra, India in 2021, Cited 55. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A thermal O-to-C [1,3]-rearrangement of alpha-hydroxy acid derived enol ethers was achieved under mild conditions. The 2-aminothiophenol protection of carboxylic acids facilitates formation of the [1,3] precursor and its thermal rearrangement via stabilization of a radical intermediate. Experimental and theoretical evidence for dissociative radical pair formation, its captodative stability via aminothiophenol, and a unique solvent effect are presented. The aminothiophenol was deprotected from rearrangement products as well as after derivatization to useful synthons.

Safety of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Alam, MN; Dash, SR; Mukherjee, A; Pandole, S; Marelli, UK; Vanka, K; Maity, P or concate me.

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Name: (4-Methoxyphenyl)methanol. 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.

Name: (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Rerkrachaneekorn, T; Tankam, T; Sukwattanasinitt, M; Wacharasindhu, S or concate me.

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Formula: C8H10O2. Recently I am researching about SOLUBLE RECEPTOR TIE-2; CARDIOVASCULAR MORTALITY; ANGPTL4; DISEASE; RISK; ANGIOGENESIS; BIOMARKER; EVENTS, Saw an article supported by the . Published in WILEY in HOBOKEN ,Authors: Aarsetoy, R; Ueland, T; Aukrust, P; Michelsen, AE; de la Fuente, RL; Ponitz, V; Brugger-Andersen, T; Grundt, H; Staines, H; Nilsen, DWT. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

Background Plasma levels of angiopoietin-2 (ANGPT2) and angiopoietin-like 4 protein (ANGPTL4) reflect different pathophysiological aspects of cardiovascular disease. We evaluated their association with outcome in a hospitalized Norwegian patient cohort (n = 871) with suspected acute coronary syndrome (ACS) and validated our results in a similar Argentinean cohort (n = 982). Methods A cox regression model, adjusting for traditional cardiovascular risk factors, was fitted for ANGPT2 and ANGPTL4, respectively, with all-cause mortality and cardiac death within 24 months and all-cause mortality within 60 months as the dependent variables. Results At 24 months follow-up, 138 (15.8%) of the Norwegian and 119 (12.1%) of the Argentinian cohort had died, of which 86 and 66 deaths, respectively, were classified as cardiac. At 60 months, a total of 259 (29.7%) and 173 (17.6%) patients, respectively, had died. ANGPT2 was independently associated with all-cause mortality in both cohorts at 24 months [hazard ratio (HR) 1.27 (95% confidence interval (CI), 1.08-1.50) for Norway, and HR 1.57 (95% CI, 1.27-1.95) for Argentina], with similar results at 60 months [HR 1.19 (95% CI, 1.05-1.35) (Norway), and HR 1.56 (95% CI, 1.30-1.88) (Argentina)], and was also significantly associated with cardiac death [HR 1.51 (95% CI, 1.14-2.00)], in the Argentinean population. ANGPTL4 was significantly associated with all-cause mortality in the Argentinean cohort at 24 months [HR 1.39 (95% CI, 1.15-1.68)] and at 60 months [HR 1.43 (95% CI, 1.23-1.67)], enforcing trends in the Norwegian population. Conclusions ANGPT2 and ANGPTL4 were significantly associated with outcome in similar ACS patient cohorts recruited on two continents. Clinical Trial Registration ClinicalTrials.gov Identifier: NCT00521976. ClinicalTrials.gov Identifier: NCT01377402.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Aarsetoy, R; Ueland, T; Aukrust, P; Michelsen, AE; de la Fuente, RL; Ponitz, V; Brugger-Andersen, T; Grundt, H; Staines, H; Nilsen, DWT or concate me.. Formula: C8H10O2

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Recently I am researching about N-PROPYLAMMONIUM PERRUTHENATE; ALCOHOLS, Saw an article supported by the Yasouj University; Iran National Science Foundation (INSF)Iran National Science Foundation (INSF). Quality Control of (4-Methoxyphenyl)methanol. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Mirbagheri, R; Elhamifar, D; Hajati, S. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

A novel method was used to prepare a magnetic phenylene-based periodic mesoporous organosilica nanocomposite with yolk-shell structure (Fe3O4@YSPMO). The Fe3O4@YSPMO nanomaterial was prepared by using easily accessible pluronic-P123 and cetyltrimethylammonium bromide (CTAB) surfactants under basic conditions. This material was employed for effective immobilization of potassium perruthenate to prepare an Fe3O4@YSPMO@Ru nanocatalyst for the aerobic oxidation of alcohols. The physiochemical properties of the designed Fe3O4@YSPMO@Ru nanocomposite were studied using PXRD, FT-IR, TGA, SEM, TEM, ICP, VSM and XPS analyses. Fe3O4@YSPMO@Ru was effectively employed as a highly recoverable nanocatalyst in the selective aerobic oxidation of alcohols.

Quality Control of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Mirbagheri, R; Elhamifar, D; Hajati, S or concate me.

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I found the field of Chemistry; Science & Technology – Other Topics very interesting. Saw the article Bioinspired Radical-Mediated Transition-Metal-Free Synthesis of N-Heterocycles under Visible Light published in 2021. Application In Synthesis of (4-Methoxyphenyl)methanol, Reprint Addresses Adhikari, D (corresponding author), Indian Inst Sci Educ & Res IISER Mohali, Dept Chem Sci, Sas Nagar 140306, Punjab, India.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

A redox-active iminoquinone motif connected with pi-delocalized pyrene core has been reported that can perform efficient two-electron oxidation of a class of substrates. The design of the molecule was inspired by the organic redox cofactor topaquinone (TPQ), which executes amine oxidation in the enzyme, copper amine oxidase. Easy oxidation of both primary and secondary alcohols happened in the presence of catalytic KOtBu, which could reduce the ligand backbone to its iminosemiquinonate form under photoinduced conditions. Moreover, this easy oxidation of alcohols under aerobic condition could be elegantly extended to multi-component, one-pot coupling for the synthesis of quinoline and pyrimidine. This organocatalytic approach is very mild (70 degrees C, 8 h) compared to a multitude of transition-metal catalysts that have been used to prepare these heterocycles. A detailed mechanistic study proves the intermediacy of the iminosemiquinonate-type radical and a critical hydrogen atom transfer step to be involved in the dehydrogenation reaction.

Application In Synthesis of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Bains, AK; Ankit, Y; Adhikari, D or concate me.

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Recommanded Product: (4-Methoxyphenyl)methanol. Authors Kon, Y; Nakashima, T; Yada, A; Fujitani, T; Onozawa, SY; Kobayashi, S; Sato, K in ROYAL SOC CHEMISTRY published article about in [Kon, Yoshihiro; Nakashima, Takuya; Yada, Akira; Fujitani, Tadahiro; Onozawa, Shun-ya; Kobayashi, Shu; Sato, Kazuhiko] Natl Inst Adv Ind Sci & Technol, Interdisciplinary Res Ctr Catalyt Chem, Tsukuba, Ibaraki 3058565, Japan; [Kobayashi, Shu] Univ Tokyo, Sch Sci, Dept Chem, Bunkyo Ku, Tokyo 1130033, Japan in 2021, Cited 41. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

The oxidation of alcohols to aldehydes is a powerful reaction pathway for obtaining valuable fine chemicals used in pharmaceuticals and biologically active compounds. Although many oxidants can oxidize alcohols, only a few hydrogen peroxide oxidations can be employed to continuously synthesize aldehydes in high yields using a liquid-liquid two-phase flow reactor, despite the possibility of the application toward a safe and rapid multi-step synthesis. We herein report the continuous flow synthesis of (E)-cinnamaldehyde from (E)-cinnamyl alcohol in 95%-98% yields with 99% selectivity for over 5 days by the selective oxidation of hydrogen peroxide using a catalyst column in which Pt is dispersed in SiO2. The active species for the developed selective oxidation is found to be zero-valent Pt(0) from the X-ray photoelectron spectroscopy measurements of the Pt surface before and after the oxidation. Using Pt black diluted with SiO2 as a catalyst to retain the Pt(0) species with the optimal substrate and H2O2 introduction rate not only enhances the catalytic activity but also maintains the activity during the flow reaction. Optimizing the contact time of the substrate with Pt and H2O2 using a flow reactor is important to proceed with the selective oxidation to prevent the catalytic H2O2 decomposition.

Recommanded Product: (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Kon, Y; Nakashima, T; Yada, A; Fujitani, T; Onozawa, SY; Kobayashi, S; Sato, K or concate me.

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Wu, D; Bu, QQ; Guo, C; Dai, B; Liu, N in [Wu, Di; Bu, Qingqing; Dai, Bin; Liu, Ning] Shihezi Univ, Sch Chem & Chem Engn, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, North Fourth Rd, Shihezi 832003, Xinjiang, Peoples R China; [Guo, Cheng] Zhejiang Univ, Affiliated Hosp 2, Sch Med, Canc Inst, Hangzhou 310009, Zhejiang, Peoples R China published Cooperative catalysis of molybdenum with organocatalysts for distribution of products between amines and imines in 2021, Cited 73. Product Details of 105-13-5. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Multi-amino groups and nitrogen donors compound was discovered as an organocatalyst for N-alkylation of alcohols with amines in the presence of Mo(CO)6. The Mo(CO)6/organocatalyst binary system has shown to be a highly active catalyst for the N-alkylation reaction between alcohols and amines with excellent tolerance of variable starting materials bearing different functional groups. Of particular note, this method possessing a superiority selectivity in the synthesis of N-alkylated amines or imines, which can be controlled by the reaction temperature. The cooperative catalysis mechanism in combination of Mo(CO)6 with organocatalyst was elucidated by control experiments.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Wu, D; Bu, QQ; Guo, C; Dai, B; Liu, N or concate me.. Product Details of 105-13-5

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I found the field of Chemistry very interesting. Saw the article Indium-Catalyzed Deoxygenation of Sulfoxides with Hydrosilanes published in 2021. Product Details of 105-13-5, Reprint Addresses Sakai, N (corresponding author), Tokyo Univ Sci RIKADAI, Fac Sci & Technol, Dept Pure & Appl Chem, Noda, Chiba 2788510, Japan.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

Described herein is that a novel InBr3/PhSiH3 reducing system in a 1,4-dioxane solution smoothly and effectively undertook deoxygenation of a variety of sulfoxides leading to the facile preparation of sulfide derivatives. Also, it was demonstrated that the reducing system shows a higher reactivity towards sulfoxides than that towards commonly reducible functional groups, such as carboxylic acids, esters, amides, and sulfones.

Product Details of 105-13-5. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Sakai, N; Shimada, R; Ogiwara, Y or concate me.

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Safety of (4-Methoxyphenyl)methanol. Recently I am researching about DEPENDENT AMINE OXIDASES; AEROBIC OXIDATION; CATALYTIC MECHANISM; ALCOHOL OXIDATION; TOPA QUINONE; ACTIVE-SITE; COPPER; HYDROGEN; MODEL; PYRIMIDINES, Saw an article supported by the SERB (DST), India [ECR/2017/001764]; IISER Mohali. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Bains, AK; Ankit, Y; Adhikari, D. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

A redox-active iminoquinone motif connected with pi-delocalized pyrene core has been reported that can perform efficient two-electron oxidation of a class of substrates. The design of the molecule was inspired by the organic redox cofactor topaquinone (TPQ), which executes amine oxidation in the enzyme, copper amine oxidase. Easy oxidation of both primary and secondary alcohols happened in the presence of catalytic KOtBu, which could reduce the ligand backbone to its iminosemiquinonate form under photoinduced conditions. Moreover, this easy oxidation of alcohols under aerobic condition could be elegantly extended to multi-component, one-pot coupling for the synthesis of quinoline and pyrimidine. This organocatalytic approach is very mild (70 degrees C, 8 h) compared to a multitude of transition-metal catalysts that have been used to prepare these heterocycles. A detailed mechanistic study proves the intermediacy of the iminosemiquinonate-type radical and a critical hydrogen atom transfer step to be involved in the dehydrogenation reaction.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Bains, AK; Ankit, Y; Adhikari, D or concate me.. Safety of (4-Methoxyphenyl)methanol

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Authors Li, DF; Wang, JG; Xu, FX; Zhang, NC; Men, Y in ROYAL SOC CHEMISTRY published article about EXPOSED 001 FACETS; SOOT OXIDATION ACTIVITY; VISIBLE PHOTOCATALYST; DOPED TIO2; PERCENTAGE; NANOCOMPOSITES; PERFORMANCE; NANOSHEETS; CATALYSTS; CRYSTALS in [Li, Dianfeng; Wang, Jinguo; Xu, Fengxia; Zhang, Nianchen; Men, Yong] Shanghai Univ Engn Sci, Sch Chem & Chem Engn, Shanghai 201620, Peoples R China in 2021, Cited 46. Recommanded Product: 105-13-5. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Selective conversion of aromatic alcohols to value-added chemicals is becoming an emerging research hotspot in heterogeneous photocatalysis, but its critical challenge is how to construct highly efficient photocatalysts. Herein, mesoporous (001)-TiO2 nanocrystals with tailored Ti3+ and surface oxygen vacancies have been fabricated by a facile hydrothermal route, showing remarkably boosted photoactivity for selective conversion of aromatic alcohols to carbonyl compounds in water medium under visible-light irradiation. Results attest that the remarkably boosted photoactivity was mainly correlated with the strong synergetic effect of exposed (001) facets, Ti3+ self-doping, and surface oxygen vacancies, leading to the enhanced reactant (aromatic alcohols and O-2) activation via the high surface energy of (001) facets, the improved visible-light absorbance via the intrinsic band gap narrowing, and the escalated photoelectron-hole separation efficiency via Ti3+ and surface oxygen vacancies acting as electron sinks. Meanwhile, a plausible photocatalytic mechanism for selective conversion of aromatic alcohols to carbonyl compounds has been elucidated in detail based on active species identified by capture experiments. It is hoped that this work can deliver some new insights into the rational design of highly efficient photocatalysts applied in future green organic selective transformation reactions.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Li, DF; Wang, JG; Xu, FX; Zhang, NC; Men, Y or concate me.. Recommanded Product: 105-13-5

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