Author: tianli

Authors Yamamoto, Y; Ota, M; Kodama, S; Michimoto, K; Nomoto, A; Ogawa, A; Furuya, M; Kawakami, K in AMER CHEMICAL SOC published article about in [Yamamoto, Yuki; Ota, Miyuto; Kodama, Shintaro; Michimoto, Kazuki; Nomoto, Akihiro; Ogawa, Akiya] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Sakai, Osaka 5998531, Japan; [Furuya, Mitsunori; Kawakami, Kiminori] Mitsubishi Chem Corp, Sci & Innovat Ctr, Yokohama, Kanagawa 2278502, Japan in 2021, Cited 67. Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A green method for the oxidation of alcohols to carboxylic acids was developed using a novel co-catalytic system based on gold, silver, and copper catalysts. This reaction system was conducted under atmospheric oxygen in water and mild conditions to selectively oxidize 5-hydroxymethylfurfural to 2,5-furandicarboxylic acid, as a building block for polyethylene furanoate, which is a 100% bio-based, future alternative to the petroleum-based polyethylene terephthalate. Furthermore, various primary alcohols were conveniently oxidized to their corresponding carboxylic acids in up to quantitative yields.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Yamamoto, Y; Ota, M; Kodama, S; Michimoto, K; Nomoto, A; Ogawa, A; Furuya, M; Kawakami, K or concate me.. Formula: C8H10O2

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Authors Sung, K; Lee, MH; Cheong, YJ; Kim, YK; Yu, S; Jang, HY in WILEY-V C H VERLAG GMBH published article about in [Sung, Kihyuk; Lee, Mi-hyun; Cheong, Yeon-Joo; Kim, Yu Kwon; Yu, Sungju; Jang, Hye-Young] Ajou Univ, Dept Energy Syst Res, Suwon 16499, South Korea in 2021, Cited 56. HPLC of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Multi N-heterocyclic carbene(NHC)-modified iridium catalysts were employed in the beta-alkylation of alcohols; dimerization of primary alcohols (Guerbet reaction), cross-coupling of secondary and primary alcohols, and intramolecular cyclization of alcohols. Mechanistic studies of Guerbet reaction, including kinetic experiments, mass analysis, and density functional theory (DFT) calculation, were employed to explain the fast reaction promoted by bimetallic catalysts, and the dramatic reactivity increase of monometallic catalysts at the late stage of the reaction.

HPLC of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Sung, K; Lee, MH; Cheong, YJ; Kim, YK; Yu, S; Jang, HY or concate me.

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Quality Control of (4-Methoxyphenyl)methanol. Authors Wu, SP; Zhang, H; Cao, QE; Zhao, QH; Fang, WH in ROYAL SOC CHEMISTRY published article about in [Wu, Shipeng; Zhang, Hao; Cao, Qiue; Zhao, Qihua; Fang, Wenhao] Yunnan Univ, Sch Chem Sci & Technol, Key Lab Med Chem Nat Resource, Minist Educ,Funct Mol Anal & Biotransformat Key L, 2 North Cuihu Rd, Kunming 650091, Yunnan, Peoples R China; [Cao, Qiue; Fang, Wenhao] Yunnan Univ, Natl Demonstrat Ctr Expt Chem & Chem Engn Educ, Kunming 650091, Yunnan, 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

Direct oxidative coupling of alcohols with amines using a non-precious metal oxide catalyst under mild conditions is highly desirable for imine synthesis. In this work, a mesoporous Mn1ZrxOy solid solution catalyst prepared by a co-precipitation method showed excellent catalytic performance in imine synthesis from primary alcohols and amines without base additives in an air atmosphere. XRD, N-2 physisorption, H-2-TPR, O-2-TPD, EPR and XPS were comprehensively used to unravel its structural, redox and amphoteric properties that closely depended on the interaction between MnOy and ZrO2 with a variable Zr ratio. The Mn1Zr0.5Oy catalyst presented the highest fractions of Mn3+ ions and reactive oxygen species on the surface, and the highest concentrations of acidic-basic sites, which were disclosed to play important roles in activating alcohols and molecular O-2 in the rate-determining step. In the model reaction of oxidative coupling of benzyl alcohol with aniline, such enhanced features of the Mn1Zr0.5Oy catalyst can promote the intrinsic catalytic activity (iTOF of 1.87 h(-1)) and boost benzylideneaniline formation (5.56 mmol g(cat).(-1) h(-1)) based on a >99% yield at 80 degrees C respectively at a fast response. It can also work effectively at a room temperature of 30 degrees C, as well as for the gram-grade synthesis. This is one of the best results among all the MnOy-based catalysts in the literature. Moreover, this catalyst showed good stability and a wide substrate scope with good to excellent yields of imines.

Quality Control of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Wu, SP; Zhang, H; Cao, QE; Zhao, QH; Fang, WH or concate me.

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In 2021 NEW J CHEM published article about SELECTIVE OXIDATION; HIGHLY EFFICIENT; COPPER NANOPARTICLES; GALACTOSE-OXIDASE; GRAPHENE OXIDE; COMPLEXES; LIGAND; CONVERSION; CHEMISTRY; SYSTEM in [Senthilkumar, Samuthirarajan; Zhong, Wei; Natarajan, Mookan; Lu, Chunxin; Liu, Xiaoming] Jiaxing Univ, Coll Biol Chem Sci & Engn, Jiaxing, Zhejiang, Peoples R China; [Xu, Binyu] Nanchang Univ, Sch Chem, Nanchang, Jiangxi, Peoples R China in 2021, Cited 51. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. COA of Formula: C8H10O2

An efficient and green protocol for aerobic oxidation of benzylic alcohols in ethanol using Cu-I-Y zeolite catalysts assisted by TEMPO (TEMPO = 2,2,6,6-tetramethyl-1-piperidine-N-oxyl) as the radical co-catalyst in the presence of atmospheric air under mild conditions is reported. The Cu-I-Y zeolite prepared via ion exchange between CuCl and HY zeolite was fully characterized by a variety of spectroscopic techniques including XRD, XPS, SEM, EDX and HRTEM. The incorporation of Cu(i) into the 3D-framework of the zeolite rendered the catalyst with good durability. The results of repetitive runs revealed that in the first three runs, there was hardly a decline in activity and a more substantial decrease in yield was observed afterwards, while the selectivity remained almost unchanged. The loss in activity was attributed to both the formation of CuO and the bleaching of copper into the liquid phase during the catalysis, of which the formation of CuO was believed to be the major contributor since the bleaching loss for each run was negligible (<2%). In this catalytic system, except TEMPO, no other additives were needed, either a base or a ligand, which was essential in some reported catalytic systems for the oxidation of alcohols. The aerobic oxidation proceeded under mild conditions (60 degrees C, and 18 hours) to quantitatively and selectively convert a wide range of benzylic alcohols to corresponding aldehydes, which shows great potential in developing green and environmentally benign catalysts for aerobic oxidation of alcohols. The system demonstrated excellent tolerance against electron-withdrawing groups on the phenyl ring of the alcohols and showed sensitivity to steric hindrance of the substrates, which is due to the confinement of the pores of the zeolite in which the oxidation occurred. Based on the mechanism reported in the literature for homogenous oxidation, a mechanism was analogously proposed for the aerobic oxidation of benzylic alcohols catalysed by this Cu(i)-containing zeolite catalyst. COA of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Senthilkumar, S; Zhong, W; Natarajan, M; Lu, CX; Xu, BY; Liu, XM or concate me.

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Product Details of 105-13-5. In 2021 SCI REP-UK published article about MANNOSE-BINDING LECTIN; IMMUNE COMPONENT FICOLIN-3; ALL-CAUSE MORTALITY; VASCULAR COMPLICATIONS; COMPLEMENT; ASSOCIATION; MICROALBUMINURIA; POPULATION; DEFICIENCY; SEVERITY in [Ostergaard, Jakob Appel] Aarhus Univ Hosp, Dept Endocrinol & Internal Med, Aarhus, Denmark; [Ostergaard, Jakob Appel; Hansen, Troels Krarup] Aarhus Univ Hosp, Steno Diabet Ctr Aarhus, Aarhus, Denmark; [Sigfrids, Fanny Jansson; Forsblom, Carol; Dahlstrom, Emma H.; Thorn, Lena M.; Harjutsalo, Valma; Groop, Per-Henrik] Folkhalsan Res Ctr, Folkhalsan Inst Genet, Helsinki, Finland; [Sigfrids, Fanny Jansson; Forsblom, Carol; Dahlstrom, Emma H.; Thorn, Lena M.; Harjutsalo, Valma; Groop, Per-Henrik] Univ Helsinki, Nephrol, Abdominal Ctr, Helsinki, Finland; [Sigfrids, Fanny Jansson; Forsblom, Carol; Dahlstrom, Emma H.; Thorn, Lena M.; Harjutsalo, Valma; Groop, Per-Henrik] Helsinki Univ Hosp, Helsinki, Finland; [Sigfrids, Fanny Jansson; Forsblom, Carol; Dahlstrom, Emma H.; Thorn, Lena M.; Harjutsalo, Valma; Groop, Per-Henrik] Univ Helsinki, Res Program Clin & Mol Metab, Fac Med, Helsinki, Finland; [Thorn, Lena M.] Univ Helsinki, Dept Gen Practice & Primary Hlth Care, Helsinki, Finland; [Harjutsalo, Valma] Natl Inst Hlth & Welf, Helsinki, Finland; [Flyvbjerg, Allan] Capital Reg Denmark, Steno Diabet Ctr Copenhagen, Copenhagen, Denmark; [Thiel, Steffen] Aarhus Univ, Dept Biomed, Aarhus, Denmark; [Groop, Per-Henrik] Monash Univ, Cent Clin Sch, Dept Diabet, Melbourne, Vic, Australia in 2021, Cited 39. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

H-ficolin recognizes patterns on microorganisms and stressed cells and can activate the lectin pathway of the complement system. We aimed to assess H-ficolin in relation to the progression of diabetic kidney disease (DKD), all-cause mortality, diabetes-related mortality, and cardiovascular events. Event rates per 10-unit H-ficolin-increase were compared in an observational follow-up of 2,410 individuals with type 1 diabetes from the FinnDiane Study. DKD progression occurred in 400 individuals. The unadjusted hazard ratio (HR) for progression was 1.29 (1.18-1.40) and 1.16 (1.05-1.29) after adjustment for diabetes duration, sex, HbA(1c), systolic blood pressure, and smoking status. After adding triglycerides to the model, the HR decreased to 1.07 (0.97-1.18). In all, 486 individuals died, including 268 deaths of cardiovascular causes and 192 deaths of complications to diabetes. HRs for all-cause mortality and cardiovascular mortality were 1.13 (1.04-1.22) and 1.05 (0.93-1.17), respectively, in unadjusted analyses. These estimates lost statistical significance in adjusted models. However, the unadjusted HR for diabetes-related mortality was 1.19 (1.05-1.35) and 1.18 (1.02-1.37) with the most stringent adjustment level. Our results, therefore, indicate that H-ficolin predicts diabetes-related mortality, but neither all-cause mortality nor fatal/non-fatal cardiovascular events. Furthermore, H-ficolin is associated with DKD progression, however, not independently of the fully adjusted model.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Ostergaard, JA; Sigfrids, FJ; Forsblom, C; Dahlstrom, EH; Thorn, LM; Harjutsalo, V; Flyvbjerg, A; Thiel, S; Hansen, TK; Groop, PH or concate me.. Product Details of 105-13-5

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An article Switchable Synthesis of alpha,alpha-Dihalomethyl and alpha,alpha,alpha-Trihalomethyl Ketones by Metal-Free Decomposition of Enaminone C=C Double Bond WOS:000505916900001 published article about SELECTIVE SYNTHESIS; COUPLING REACTIONS; ALPHA; TRICHLOROMETHYL; CLEAVAGE; REDUCTION; ALKYNES; ALPHA,ALPHA-DIBROMOACETOPHENONES; TRIPHENYLPHOSPHINE; HYDROXYLATION in [Liu, Yunyun; Xiong, Jin; Wei, Li; Wan, Jie-Ping] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China in 2020, Cited 77. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Category: alcohols-buliding-blocks

The novel free radical-based cleavage of the enaminone C=C double bond is realized by using N-halosuccinimides (NXS) in the presence of benzoyl peroxide (BPO) with mild heating, enabling the tunable synthesis of alpha,alpha-dihalomethyl ketones and alpha,alpha,alpha-trihalomethyl ketones under different reaction conditions. The formation of these divergent products involving featured C=C double bond cleavage requires no any metal reagent, and represents one more practical example on the synthesis of poly halogenated methyl ketones via the functionalization of carbon-carbon bond.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Liu, YY; Xiong, J; Wei, L; Wan, JP or concate me.. Category: alcohols-buliding-blocks

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I found the field of Chemistry very interesting. Saw the article [(PPh3)(2)NiCl2]-Catalyzed C-N Bond Formation Reaction via Borrowing Hydrogen Strategy: Access to Diverse Secondary Amines and Quinolines published in 2021. Quality Control of (4-Methoxyphenyl)methanol, Reprint Addresses Rit, A (corresponding author), Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India.. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

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.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Donthireddy, SNR; Pandey, VK; Rit, A or concate me.. Quality Control of (4-Methoxyphenyl)methanol

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Name: (4-Methoxyphenyl)methanol. Authors Wu, SP; Zhang, H; Cao, QE; Zhao, QH; Fang, WH in ROYAL SOC CHEMISTRY published article about in [Wu, Shipeng; Zhang, Hao; Cao, Qiue; Zhao, Qihua; Fang, Wenhao] Yunnan Univ, Sch Chem Sci & Technol, Key Lab Med Chem Nat Resource, Minist Educ,Funct Mol Anal & Biotransformat Key L, 2 North Cuihu Rd, Kunming 650091, Yunnan, Peoples R China; [Cao, Qiue; Fang, Wenhao] Yunnan Univ, Natl Demonstrat Ctr Expt Chem & Chem Engn Educ, Kunming 650091, Yunnan, 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

Direct oxidative coupling of alcohols with amines using a non-precious metal oxide catalyst under mild conditions is highly desirable for imine synthesis. In this work, a mesoporous Mn1ZrxOy solid solution catalyst prepared by a co-precipitation method showed excellent catalytic performance in imine synthesis from primary alcohols and amines without base additives in an air atmosphere. XRD, N-2 physisorption, H-2-TPR, O-2-TPD, EPR and XPS were comprehensively used to unravel its structural, redox and amphoteric properties that closely depended on the interaction between MnOy and ZrO2 with a variable Zr ratio. The Mn1Zr0.5Oy catalyst presented the highest fractions of Mn3+ ions and reactive oxygen species on the surface, and the highest concentrations of acidic-basic sites, which were disclosed to play important roles in activating alcohols and molecular O-2 in the rate-determining step. In the model reaction of oxidative coupling of benzyl alcohol with aniline, such enhanced features of the Mn1Zr0.5Oy catalyst can promote the intrinsic catalytic activity (iTOF of 1.87 h(-1)) and boost benzylideneaniline formation (5.56 mmol g(cat).(-1) h(-1)) based on a >99% yield at 80 degrees C respectively at a fast response. It can also work effectively at a room temperature of 30 degrees C, as well as for the gram-grade synthesis. This is one of the best results among all the MnOy-based catalysts in the literature. Moreover, this catalyst showed good stability and a wide substrate scope with good to excellent yields of imines.

Name: (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Wu, SP; Zhang, H; Cao, QE; Zhao, QH; Fang, WH or concate me.

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COA of Formula: C8H10O2. Kobayashi, F; Fujita, M; Ide, T; Ito, Y; Yamashita, K; Egami, H; Hamashima, Y in [Kobayashi, Fumihisa; Fujita, Masashi; Ide, Takafumi; Ito, Yuta; Yamashita, Kenji; Egami, Hiromichi; Hamashima, Yoshitaka] Univ Shizuoka, Sch Pharmaceut Sci, Suruga Ku, Shizuoka 4228526, Japan published Dual-Role Catalysis by Thiobenzoic Acid in C alpha-H Arylation under Photoirradiation in 2021, Cited 70. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Thiobenzoic acid (TBA) can serve as a single-electron reducing agent under photoirradiation from a blue light-emitting diode, in the presence of appropriate electron acceptors, and the resulting sulfur-centered radical species undergoes hydrogen atom abstraction. This dual-role catalysis by TBA enables regioselectivie C alpha-H arylation of benzylamines, benzyl alcohols, and ethers, as well as dihydroimidazoles, with cyano(hetero)arenes in good yield, without the need for a transition-metal photocatalyst and/or synthetically elaborated organic dyes.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Kobayashi, F; Fujita, M; Ide, T; Ito, Y; Yamashita, K; Egami, H; Hamashima, Y or concate me.. COA of Formula: C8H10O2

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In 2021 NEW J CHEM published article about C BOND FORMATION; ALPHA-ALKYLATION; UNACTIVATED AMIDES; KETONES; METHYLATION; ESTERS; ARYLACETONITRILES; FUNCTIONALIZATION; COMPLEXES; METHANOL in [Hu, Miao; Jiang, Yong; Sun, Nan; Hu, Baoxiang; Shen, Zhenlu; Hu, Xinquan; Jin, Liqun] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310032, Peoples R China; [Jin, Liqun] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China in 2021, Cited 65. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Application In Synthesis of (4-Methoxyphenyl)methanol

An efficient method for the Ni-catalyzed C3-alkylation of indoles using readily available alcohols as the alkylating reagents has been developed. The alkylation was addressed with an air and moisture-stable binuclear nickel complex ligated by tetrahydroquinolin-8-one as the effective pre-catalyst. The newly developed transformation could accommodate a broad substrate scope including primary/secondary benzylic and aliphatic alcohols and substituted indoles. Mechanistic studies suggested that the reaction proceeds through a borrowing hydrogen pathway.

Application In Synthesis of (4-Methoxyphenyl)methanol. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Hu, M; Jiang, Y; Sun, N; Hu, BX; Shen, ZL; Hu, XQ; Jin, LQ or concate me.

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