Category: 105-13-5

Quality Control of (4-Methoxyphenyl)methanol. Fernandes, RA; Sampaio, MJ; Da Silva, ES; Boumeriame, H; Lopes, T; Andrade, L; Mendes, A; Faria, JL; Silva, CG in [Fernandes, Raquel A.; Sampaio, Maria J.; Da Silva, Eliana S.; Boumeriame, Hanane; Faria, Joaquim L.; Silva, Claudia G.] Univ Porto, Fac Engn, Associate Lab LSRE LCM, Rua Dr Roberto Frias S-N, P-4200465 Porto, Portugal; [Boumeriame, Hanane] Univ Abdelmalek Essaadi, Fac Sci & Tech, Lab Chem Engn & Valorizat Resources LGCVR UAE L01, Tangier, Morocco; [Lopes, Tania; Andrade, Luisa; Mendes, Adelio] Univ Porto, Fac Engn, LEPABE Lab Proc Engn Environm Biotechnol & Energy, Rua Dr Roberto Frias, P-4200465 Porto, Portugal published Sustainable production of value-added chemicals and fuels by using a citric acid-modified carbon nitride optical semiconductor in 2021, Cited 70. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Citric acid-modified graphite-like carbon nitride materials (GCN-zCA) were synthetized by thermal copolymerization of dicyandiamide with different amounts of citric acid (z = between 5 and 25 mg). The resulting materials presented surface porosity, defective polymeric structure, and enhanced visible light absorption in the 450-700 nm range, attributed to the existence of mid-gap states and n-pi* electronic transitions. All the modified catalysts presented high selectivity (>99 %) towards the conversion of p-anisyl alcohol into p-anisaldehyde under visible-LED irradiation, the best performing photocatalyst (GCN-20CA) reaching 63 % yield (contrasting with 22 % obtained with bulk GCN) after 240 min reaction. GCN-20CA was also applied for hydrogen generation from water splitting. The modified material practically duplicated the hydrogen production when compared to bulk GCN (75 and 44 mu mol H-2 evolved in three hours, respectively), by using platinum nanoparticles as co-catalyst and EDTA as sacrificial electron donor. Moreover, p-anisyl alcohol was successfully used as sacrificial agent for water splitting, with simultaneous production of p-anisaldehyde and H-2. Reusability tests showed that GCN-20CA remained stable in a series of consecutive runs both for p-anisaldehyde synthesis and hydrogen production.

Welcome to talk about 105-13-5, If you have any questions, you can contact Fernandes, RA; Sampaio, MJ; Da Silva, ES; Boumeriame, H; Lopes, T; Andrade, L; Mendes, A; Faria, JL; Silva, CG or send Email.. Quality Control of (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Recommanded Product: 105-13-5. In 2021 J VASC ACCESS published article about BLOOD-STREAM INFECTION; VASCULAR ACCESS; PREVENTION; DEVICES; REMOVAL; ADULTS in [Chiaretti, Antonio; Sassudelli, Giovanni; Gatto, Antonio] Fdn Policlin Univ Agostino Gemelli, Dept Pediat, IRCCS, Rome, Italy; [Pittiruti, Mauro] Fdn Policlin Univ Agostino Gemelli, Dept Surg, IRCCS, Rome, Italy; [Conti, Giorgio; Pulitano, Silvia Maria; Mancino, Aldo] Fdn Policlin Univ Agostino Gemelli, Pediat Intens Care Unit, IRCCS, Rome, Italy; [Rossi, Marco; Pusateri, Angela; Tosi, Federica] Fdn Policlin Univ Agostino Gemelli, Dept Anesthesia & Pain Therapy, IRCCS, Rome, Italy in 2021, Cited 25. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Background: Placement of central venous access devices is a clinical procedure associated with some risk of adverse events and with a relevant cost. Careful choice of the device, appropriate insertion technique, and proper management of the device are well-known strategies commonly adopted to achieve an optimal clinical result. However, the environment where the procedure takes place may have an impact on the overall outcome in terms of safety and cost-effectiveness. Methods: We carried out a retrospective analysis on pediatric patients scheduled for a major neurosurgical operation, who required a central venous access device in the perioperative period. We divided the patients in two groups: in group A the central venous access device was inserted in the operating room, while in group B the central venous access device was inserted in the sedation room of our Pediatric Intensive Care Unit. We compared the two groups in terms of safety and cost-effectiveness. Results: We analyzed 47 central venous access devices in 42 children. There were no insertion-related complications. Only one catheter-related bloodstream infection was recorded, in group A. However, the costs related to central venous access device insertion were quite different: euro330-euro540 in group A versus euro105-euro135 in group B. Conclusion: In the pediatric patient candidate to a major neurosurgical operation, preoperative insertion of the central venous access device in the sedation room rather than in the operating room is less expensive and equally safe.

Recommanded Product: 105-13-5. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Chiaretti, A; Pittiruti, M; Sassudelli, G; Conti, G; Rossi, M; Pulitano, SM; Mancino, A; Pusateri, A; Gatto, A; Tosi, F or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Application In Synthesis of (4-Methoxyphenyl)methanol. Authors Jin, B; Wang, JG; Xu, FX; Li, DF; Men, Y in ELSEVIER published article about in [Jin, Bei; Wang, Jinguo; Xu, Fengxia; Li, Dianfeng; Men, Yong] Shanghai Univ Engn Sci, Sch Chem & Chem Engn, Shanghai 201620, Peoples R China in 2021, Cited 59. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Selective conversion of biomass-derived alcohols into carbonyl compounds via visible-light photocatalysis is realized over hierarchical hollow WO3 microspheres with tailored surface oxygen vacancies, which presents the remarkably boosted photoactivity in terms of selectivity and activity, intrinsically attributing to the strong synergetic effect of hierarchical spherical cavity and surface oxygen vacancies simultaneously. The hierarchical spherical cavity, substantially constructed by the self-interconnected nanosheets, enhances the light-harvesting ability via multiple light reflections not only in spherical cavity but also among the self-interconnected nanosheets. Surface oxygen vacancies favor the energy band gap narrowing via forming a miniband just below the conduction band and then extend the photoresponse region, further boosting the light-harvesting ability. Importantly, surface oxygen vacancies function as the electron sinks to capture photoelectrons and thus restrict their recombination probability with holes, finally improving the photoelectron-hole separation efficiency. Meanwhile, this photocatalyst presents excellent reusability, showing its promising potential in practical applications. This work sheds light on a new application of hierarchical WO3 microspheres with tailored surface oxygen vacancies and its strong synergetic effect of hierarchical structures and surface oxygen vacancies on photocatalytic performance, delivering new insights for rationally designing highly active photocatalysts applied in future green and sustainable organic transformation reactions.

Welcome to talk about 105-13-5, If you have any questions, you can contact Jin, B; Wang, JG; Xu, FX; Li, DF; Men, Y or send Email.. Application In Synthesis of (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

An article Synthesis of functionalized pyrimidouracils by ruthenium-catalyzed oxidative insertion of (hetero)aryl methanols into N-uracil amidines WOS:000587048900001 published article about ONE-POT SYNTHESIS; HETEROCYCLIZATION SYNTHESIS; NITROGEN-HETEROCYCLES; 3-COMPONENT SYNTHESIS; PURINE DERIVATIVES; AEROBIC OXIDATION; EFFICIENT; ALCOHOLS; ALDEHYDES; 1,3,5-TRIAZINES in [Debnath, Pradip] Maharaja Bir Bikram Coll, Dept Chem, Agartala 799004, Tripura, India; [Sahu, Gouranga] Ramkrishna Mahavidyalaya, Dept Chem, Unakoti, India; [De, Utpal C.] Tripura Univ, Dept Chem, Agartala, India in 2021, Cited 96. 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

A dehydrogenative coupling of N-uracil amidines with (hetero)aryl methanols has been developed, allowing for the facile synthesis of a broad range of structurally diverse pyrimidouracils. By applying [RuCl2(p-cymene)](2)/Cs2CO3 as an efficient catalytic system, the easily available, cheap (hetero)aryl methanols were firstly employed for oxidative insertion/C-H amination into the N-uracil amidines, providing highly functionalized pyrimido[4,5-d]pyrimidine-2,4-diones. Due to the better stability of alcohols than aldehydes, this synthetic protocol is applicable to a broad range of alcoholic substrates and does not required any protection during the whole preparation process. The presented protocol has the potential to prepare valuable products which cannot be accessed presently or extremely arduous to procure by following regular procedure. Hence, this is a remarkably improved protocol compared with the existing methodologies. The overall reaction sequence is an effective oxidation-imination-cyclization tandem process catalyzed by ruthenium catalyst.

Welcome to talk about 105-13-5, If you have any questions, you can contact Debnath, P; Sahu, G; De, UC or send Email.. Product Details of 105-13-5

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

An article A General and Selective Synthesis of Methylmonochlorosilanes from Di-, Tri-, and Tetrachlorosilanes WOS:000643163800063 published article about CROSS-COUPLING REACTION; GRIGNARD REACTION; ARYL BROMIDES; VINYL HALIDES; SILANES; SILICON; ELECTROPHILES; CHLOROSILANES; PRECATALYST; METHYLATION in [Naganawa, Yuki; Sakamoto, Kei; Nakajima, Yumiko] Natl Inst Adv Ind Sci & Technol, Interdisciplinary Res Ctr Catalyt Chem IRC3, Tsukuba, Ibaraki 3058565, Japan in 2021, Cited 50. Quality Control of (4-Methoxyphenyl)methanol. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

Direct catalytic transformation of chlorosilanes into organosilicon compounds remains challenging due to difficulty in cleaving the strong Si-Cl bond(s). We herein report the palladium-catalyzed cross-coupling reaction of chlorosilanes with organoaluminum reagents. A combination of [Pd(C3H5)Cl](2) and DavePhos ligand catalyzed the selective methylation of various dichlorosilanes 1, trichlorosilanes 5, and tetrachlorosilane 6 to give the corresponding monochlorosilanes.

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.. Quality Control of (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

An article Nano NiFe 2 O 4 supported phenanthroline Cu(II) complex as a retrievable catalyst for selective and environmentally friendly oxidation of benzylic alcohols WOS:000647557500013 published article about NICKEL FERRITE NANOPARTICLES; AEROBIC OXIDATION; MAGNETIC NANOPARTICLES; MECHANISM; ALDEHYDES; EFFICIENT; LIGAND in [Mehrjoyan, Forouzan] Islamic Azad Univ, Dept Chem, Ahvaz Branch, Ahvaz, Iran; [Afshari, Mozhgan] Islamic Azad Univ, Dept Chem, Shoushtar Branch, Shoushtar 6451741117, Iran in 2021, Cited 34. 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

A new magnetically recoverable catalyst consisting of phenanthroline Cu(II) complex supported on nickel ferrite nanoparticles was prepared. The synthesized catalyst was characterized by Fourier transform in-frared spectroscopy, X-ray diffraction, transmission and scanning electron microscopes, thermogravimetry, energy dispersive X-ray spectroscopy, vibrating sample magnetometry and inductively coupled plasma. Supported copper complex used for solvent free oxidation of 1-phenyl ethanol as a model. Influence of the reaction parameters (kind of oxidant, amount of the catalyst, reaction time, solvent and reaction temperature) were studied. Because of the immobilized complex has been shown to be an efficient het-erogeneous catalyst for the selective oxidation of 1-phenyl ethanol to acetophenone (94% yield) by hydro-gen peroxide so this green approach extended to other benzylic alcohols. The catalyst had been reused 10 times with no significant loss of catalytic activity. SEM, EDX, XRD, and ICP analysis of reused catalyst indicated that the catalyst was stable after the reaction. (c) 2021 Published by Elsevier B.V.

Welcome to talk about 105-13-5, If you have any questions, you can contact Mehrjoyan, F; Afshari, M or send Email.. Application In Synthesis of (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

In 2021 ASIAN J ORG CHEM published article about CATALYZED SELECTIVE OXIDATION; AEROBIC OXIDATION; HYDROGEN-PEROXIDE; C-N; COPPER; METAL; ALDEHYDES; NANOPARTICLES; COMPLEXES; EFFICIENT in [Behera, Pradyota Kumar; Choudhury, Prabhupada; Sahu, Santosh Kumar; Sahu, Rashmi Ranjan; Rout, Laxmidhar] Berhampur Univ, Dept Chem, Berhampur 760007, Orissa, India; [Rout, Laxmidhar] IISER, Dept Chem, Berhampur 760010, Odisha, India; [Harvat, Alisha N.; McNulty, Caitlin; Stitgen, Abigail; Scanlon, Joseph] Ripon Coll, Ripon, WI 54971 USA; [Kar, Manoranjan] IIT Patna, Patna 801106, Bihar, India in 2021, Cited 113. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Safety of (4-Methoxyphenyl)methanol

Though concept of oxygen bridged bimetallic catalyst for organic reaction is not well understood. Herein, we have tried to explain the concept by experimental as well as its support by full DFT study. We report here a competent protocol for dehydrogenative oxidation of benzylic alcohol using an oxygen bridged bimetallic CuMoO4 nano catalyst. Careful demonstration reveals that oxidation is not effective either with mono-metallic Cu (II) or Mo(VI); instead combination of both the metals through the oxygen bridge [Cu-O-Mo] unexpectedly and interestingly catalyzed the reaction efficiently. The new concept is strongly supported by computational DFT study. DFT study reveals dehydrogenative oxidation is preferred at copper centre over molybdenum and aromatic benzyl alcohols are greatly stabilised. Interaction barrier energy of monometallic CuO and MoO3 catalyst is much higher than bimetallic CuMoO4. Hydrogen transfer has larger barrier heights for CuO (31.5 kcal/mol) and MoO3 (40.3 kcal/mol) than bimetallic CuMoO4.

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.. Safety of (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

An article Mimicking transition metals in borrowing hydrogen from alcohols WOS:000652242100001 published article about CATALYZED N-ALKYLATION; C-C; AMINES; PHENALENYL; SPIN; EFFICIENT; AMIDES; HYDROAMINATION; ARYLAMINES; CHEMISTRY in [Banik, Ananya; Ahmed, Jasimuddin; Sil, Swagata; Mandal, Swadhin K.] Indian Inst Sci Educ & Res Kolkata, Dept Chem Sci, Mohanpur 741246, India in 2021, Cited 68. 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

Borrowing hydrogen from alcohols, storing it on a catalyst and subsequent transfer of the hydrogen from the catalyst to an in situ generated imine is the hallmark of a transition metal mediated catalytic N-alkylation of amines. However, such a borrowing hydrogen mechanism with a transition metal free catalytic system which stores hydrogen molecules in the catalyst backbone is yet to be established. Herein, we demonstrate that a phenalenyl ligand can imitate the role of transition metals in storing and transferring hydrogen molecules leading to borrowing hydrogen mediated alkylation of anilines by alcohols including a wide range of substrate scope. A close inspection of the mechanistic pathway by characterizing several intermediates through various spectroscopic techniques, deuterium labelling experiments, and DFT study concluded that the phenalenyl radical based backbone sequentially adds H+, H and an electron through a dearomatization process which are subsequently used as reducing equivalents to the C-N double bond in a catalytic fashion.

Product Details of 105-13-5. Welcome to talk about 105-13-5, If you have any questions, you can contact Banik, A; Ahmed, J; Sil, S; Mandal, SK or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Riadi, Y in [Riadi, Yassin] Prince Sattam Bin Abdulaziz Univ, Coll Pharm, Dept Pharmaceut Chem, Al Kharj, Saudi Arabia published UV Light Mediated Palladium-Catalyzed Synthesis of 2-Substituedpyrido[2,3-d]pyrimidines in 2021, Cited 26. COA of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

A novel and effective photochemical approach for access to 2-substituted pyrido[2,3-d]pyrimidines is described starting from the corresponding 2-(2-aminopyridin-3-yl)ethenol through a palladium-catalyzed reaction. Our strategy involves an original procedure under UV light as source of energy with reaction times of 24-36 h and yields ranging between 42 and 92%.

COA of Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Riadi, Y or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

In 2021 ACS CATAL published article about PHOTOREDOX CATALYSIS; BOND FUNCTIONALIZATION; ACTIVATION; STRATEGY; TETRAHYDROISOQUINOLINES; ORGANOCATALYSIS; ALKYLATION; PHOTOLYSIS; CYANATION; RADICALS 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 in 2021, Cited 70. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5. Formula: C8H10O2

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.

Formula: C8H10O2. Welcome to talk about 105-13-5, If you have any questions, you can contact Kobayashi, F; Fujita, M; Ide, T; Ito, Y; Yamashita, K; Egami, H; Hamashima, Y or send Email.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts