Brief introduction of (4-Methoxyphenyl)methanol

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.

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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An update on the compound challenge: 105-13-5

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

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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You Should Know Something about (4-Methoxyphenyl)methanol

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.

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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Extended knowledge of (4-Methoxyphenyl)methanol

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

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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How did you first get involved in researching (4-Methoxyphenyl)methanol

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

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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Downstream Synthetic Route Of 105-13-5

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

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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Why Are Children Getting Addicted To (4-Methoxyphenyl)methanol

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Tsai, WL; Nash, MS; Rosenbaum, DJ; Prince, SE; D’Aloisio, AA; Neale, AC; Sandler, DP; Buckley, TJ; Jackson, LE or concate me.. Product Details of 105-13-5

An article Types and spatial contexts of neighborhood greenery matter in associations with weight status in women across 28 US communities WOS:000663724900007 published article about ECOSYSTEM SERVICES; PHYSICAL-ACTIVITY; RESIDENTIAL GREENNESS; OBESITY; SPACE; WALKING; HEALTH; COHORT; CLASSIFICATION; ACCESSIBILITY in [Tsai, Wei-Lun; Rosenbaum, Daniel J.; Prince, Steven E.; Neale, Anne C.; Buckley, Timothy J.; Jackson, Laura E.] US EPA, Off Res & Dev, Res Triangle Pk, NC 27711 USA; [Nash, Maliha S.] US EPA, Off Res & Dev, Newport, OR USA; [D’Aloisio, Aimee A.] Social & Sci Syst, Durham, NC USA; [Sandler, Dale P.] NIEHS, POB 12233, Res Triangle Pk, NC 27709 USA in 2021, Cited 72. 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

Excess body weight is a risk factor for many chronic diseases. Studies have identified neighborhood greenery as supportive of healthy weight. However, few have considered plausible effect pathways for ecosystem services (e. g., heat mitigation, landscape aesthetics, and venues for physical activities) or potential variations by climate. This study examined associations between weight status and neighborhood greenery that capture ecosystem services most relevant to weight status across 28 U.S. communities. Weight status was defined by body mass index (BMI) reported for 6591 women from the U.S. Sister Study cohort. Measures of greenery within street and circular areas at 500 m and 2000 m buffer distances from homes were derived for each participant using 1 m land cover data. Street area was defined as a 25 m-wide zone on both sides of street centerlines multiplied by the buffer distances, and circular area was the area of the circle centered on a home within each of the buffer distances. Measures of street greenery characterized the pedestrian environment to capture physically and visually accessible greenery for shade and aesthetics. Circular greenery was generated for comparison. Greenery types of tree and herbaceous cover were quantified separately, and a combined measure of tree and herbaceous cover (i.e., aggregate greenery) was also included. Mixed models accounting for the clustering at the community level were applied to evaluate the associations between neighborhood greenery and the odds of being overweight or obese (BMI > 25) with adjustment for covariates selected using gradient boosted regression trees. Analyses were stratified by climate zone (arid, continental, and temperate). Tree cover was consistently associated with decreased odds of being overweight or obese. For example, the adjusted odds ratio [AOR] was 0.92, 95% Confidence Interval [CI]: 0.88-0.96, given a 10% increase in street tree cover at the 2000 m buffer across the 28 U.S. communities. These associations held across climate zones, with the lowest AOR in the arid climate (AOR: 0.74, 95% CI: 0.54-1.01). In contrast, associations with herbaceous cover varied by climate zone. For the arid climate, a 10% increase in street herbaceous cover at the 2000 m buffer was associated with lower odds of being overweight or obese (AOR: 0.75, 95% CI: 0.55-1.03), whereas the association was reversed for the temperate climate, the odds increased (AOR: 1.19, 95% CI: 1.05-1.35). Associations between greenery and overweight/obesity varied by type and spatial context of greenery, and climate. Our findings add to a growing body of evidence that greenery design in urban planning can support public health. These findings also justify further defining the mechanism that underlies the observed associations.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Tsai, WL; Nash, MS; Rosenbaum, DJ; Prince, SE; D’Aloisio, AA; Neale, AC; Sandler, DP; Buckley, TJ; Jackson, LE or concate me.. Product Details of 105-13-5

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Extracurricular laboratory: Synthetic route of 105-13-5

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.

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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Let`s talk about compound :(4-Methoxyphenyl)methanol

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.

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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A new application about(4-Methoxyphenyl)methanol

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

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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