Tag: M.W=100-150

An article Fe Doped MIL-101/Graphene Nanohybrid for Photocatalytic Oxidation of Alcohols Under Visible-Light Irradiation WOS:000604191700004 published article about METAL-ORGANIC FRAMEWORK; SELECTIVE OXIDATION; AROMATIC ALCOHOLS; HYDROGEN-PRODUCTION; REACTIVE DYE; NANOCOMPOSITE; EFFICIENT; MIL-101; NANOPARTICLES; PERFORMANCE in [Wang, Mingming; Ma, Yali; Lv, Bolin; Hua, Fenglin; Meng, Shuangyan; Lei, Xuedi; Wang, Qingtao; Su, Bitao; Lei, Ziqiang; Yang, Zhiwang] Northwest Normal Univ, Coll Chem & Chem Engn, Key Lab Polymer Mat Gansu Prov, Key Lab Ecofunct Polymer Mat,Minist Educ, Lanzhou 730070, Peoples R China in 2021, Cited 44. Name: (4-Methoxyphenyl)methanol. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A novel photoactive porous material of GR/FeMIL-101 based on FeMIL-101 metal organic frameworks (MOFs) was successfully synthesized via a simple hydrothermal method. The structural and photoelectric properties of the GR/FeMIL-101 was analyzed by XRD, SEM, TEM, TGA, XPS, UV-vis DRS, FT-IR, PL and EIS methods. The photocatalytic performance for the selective oxidation of benzyl alcohol with GR/FeMIL-101 as catalysts was evaluated under visible light irradiation. The results showed that the GR/FeMIL-101 nanohybrid had better photocatalytic performance than both of FeMIL-101 and the pristine MIL-101. It was further found that the incorporation of Fe and MIL-101 caused valence fluctuations of Fe3+/Fe2+ which improved the absorption of visible-light and increased the separation efficiency of photogenerated charges. In addition, the combination of FeMIL-101 and GR could further promote the transfer rate of the photoelectrons. The mechanism of the reaction revealed that center dot O-2(-) was the dominating active specie in this reaction through active species trapping experiments. [GRAPHICS] .

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Wang, MM; Ma, YL; Lv, BL; Hua, FL; Meng, SY; Lei, XD; Wang, QT; Su, BT; Lei, ZQ; Yang, ZW or concate me.. Name: (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Computed Properties of C8H10O2. 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. 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.

Computed Properties of C8H10O2. 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.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

In 2021 APPL ORGANOMET CHEM 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. Safety of (4-Methoxyphenyl)methanol

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.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Debnath, P; Sahu, G; De, UC or concate me.. Safety of (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

SDS of cas: 105-13-5. Authors Jeong, J; Fujita, K in AMER CHEMICAL SOC published article about in [Jeong, Jaeyoung; Fujita, Ken-ichi] Kyoto Univ, Grad Sch Human & Environm Studies, Kyoto 6068501, Japan in 2021, Cited 70. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

A new catalytic system for N,N-dimethylamination of primary alcohols using aqueous dimethylamine in the absence of additional organic solvents has been developed. The reaction proceeds via borrowing hydrogen processes, which are atom-efficient and environmentally benign. An iridium catalyst bearing an N-heterocyclic carbene (NHC) ligand exhibited high performance, without showing any deactivation under aqueous conditions. In addition, valuable N,N-dimethylamine derivatives, including biologically active and pharmaceutical molecules, were synthesized. The practical application of this methodology was demonstrated by a gram-scale reaction.

SDS of cas: 105-13-5. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Jeong, J; Fujita, K or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Category: alcohols-buliding-blocks. Recently I am researching about BIS(IMINO)PYRIDINE COBALT COMPLEXES; CHEMOSELECTIVE HYDROGENATION; IRON; EFFICIENT; SOLVENT; AMIDES; MILD; HYDROBORATION; ISOMERIZATION; INHIBITION, Saw an article supported by the CSIR, New DelhiCouncil of Scientific & Industrial Research (CSIR) – India [01(2942)/18/EMR-II]; MHRD; DST/INSPIRE fellowship [IF160793]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Singh, A; Maji, A; Joshi, M; Choudhury, AR; Ghosh, K. The CAS is 105-13-5. Through research, I have a further understanding and discovery of (4-Methoxyphenyl)methanol

Base-metal catalysts Co1, Co2 and Co3 were synthesized from designed pincer ligands L-1, L-2 and L-3 having NNN donor atoms respectively. Co1, Co2 and Co3 were characterized by IR, UV-Vis. and ESI-MS spectroscopic studies. Single crystal X-ray diffraction studies were investigated to authenticate the molecular structures of Co1 and Co3. Catalysts Col, Co2 and Co3 were utilized to study the dehydrogenative activation of alcohols for N-alkylation of amines, alpha-alkylation of ketones and synthesis of quinolines. Under optimized reaction conditions, a broad range of substrates including alcohols, anilines and ketones were exploited. A series of control experiments for N-alkylation of amines, alpha-alkylation of ketones and synthesis of quinolines were examined to understand the reaction pathway. ESI-MS spectral studies were investigated to characterize cobalt-alkoxide and cobalt-hydride intermediates. Reduction of styrene by evolved hydrogen gas during the reaction was investigated to authenticate the dehydrogenative nature of the catalysts. Probable reaction pathways were proposed for N-alkylation of amines, alpha-alkylation of ketones and synthesis of quinolines on the basis of control experiments and detection of reaction intermediates.

Category: alcohols-buliding-blocks. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Singh, A; Maji, A; Joshi, M; Choudhury, AR; Ghosh, K or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Ou, W; Xiang, XD; Zou, R; Xu, Q; Loh, KP; Su, CL in [Ou, Wei; Xiang, Xudong; Zou, Ru; Su, Chenliang] Shenzhen Univ, Int Collaborat Lab 2D Mat Optoelect Sci & Technol, Engn Technol Res Ctr 2D Mat Informat Funct Device, Inst Microscale Optoelect, Shenzhen 518060, Peoples R China; [Xu, Qing] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou, Zhejiang, Peoples R China; [Loh, Kian Ping] Natl Univ Singapore, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore published Room-Temperature Palladium-Catalyzed Deuterogenolysis of Carbon Oxygen Bonds towards Deuterated Pharmaceuticals in 2021, Cited 50. COA of Formula: C8H10O2. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Site-specific incorporation of deuterium into drug molecules to study and improve their biological properties is crucial for drug discovery and development. Herein, we describe a palladium-catalyzed room-temperature deuterogenolysis of carbon-oxygen bonds in alcohols and ketones with D-2 balloon for practical synthesis of deuterated pharmaceuticals and chemicals with benzyl-site (sp(3) C-H) D-incorporation. The highlights of this deoxygenative deuteration strategy are mild conditions, broad scope, practicability and high chemoselectivity. To enable the direct use of D2O, electrocatalytic D2O-splitting is adapted to in situ supply D-2 on demand. With this system, the precise incorporation of deuterium in the metabolic position (benzyl-site) of ibuprofen is demonstrated in a sustainable and practical way with D2O.

COA of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Ou, W; Xiang, XD; Zou, R; Xu, Q; Loh, KP; Su, CL or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

COA of Formula: C8H10O2. In 2021 INORG CHIM ACTA published article about AEROBIC OXIDATION; CIS-DIOXOMOLYBDENUM(VI) COMPLEXES; MOLYBDENUM(VI) COMPLEX; HYDROGEN-PEROXIDE; MOLECULAR-OXYGEN; SC-XRD; EPOXIDATION; METAL; EFFICIENT; BENZALDEHYDE in [Kargar, Hadi] Ardakan Univ, Dept Chem Engn, Fac Engn, POB 184, Ardakan, Iran; [Forootan, Pooran; Fallah-Mehrjardi, Mehdi; Behjatmanesh-Ardakani, Reza] Payame Noor Univ, Dept Chem, Tehran 193953697, Iran; [Rudbari, Hadi Amiri] Univ Isfahan, Dept Chem, Esfahan 8174673441, Iran; [Munawar, Khurram Shahzad] Univ Sargodha, Dept Chem, Punjab, Pakistan; [Munawar, Khurram Shahzad] Univ Mianwali, Dept Chem, Mianwali, Pakistan; [Ashfaq, Muhammad; Tahir, Muhammad Nawaz] Univ Sargodha, Dept Phys, Punjab, Pakistan in 2021, Cited 98. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Two new oxovanadium and dioxomolybdenum Schiff base complexes, [VvO(L)(OCH3)(CH3OH)] and [MoVIO2(L) (CH2CH3OH)], were synthesized by treating an ONO-donor type Schiff base ligand (H2L) derived by condensation of 5-nitrosalicylaldehyde and nicotinic hydrazide with oxo and dioxo acetylacetonate salts of vanadium and molybdenum, [VO(acac)2 and MoO2(acac)2], respectively. The synthesized ligand and complexes were characterized by various spectroscopic techniques like FT-IR, multinuclear (1H, 13C) NMR, elemental analysis and the most authentic single crystal X-ray diffraction analysis. In both complexes the geometry around the central metal ions was distorted octahedral as revealed by the data collected from diffraction studies. Theoretical calculation of the synthesized compounds were carried out by DFT as well as TD-DFT using B3LYP method by employing the Def2-TZVP basis set. The findings of theoretical data indicated that the calculated results are in accordance with the experimental findings. Moreover, the catalytic efficiencies of both complexes were investigated by oxidizing the benzylic alcohols in the presence of urea hydrogen peroxide (UHP) in acetonitrile.

COA of Formula: C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Kargar, H; Forootan, P; Fallah-Mehrjardi, M; Behjatmanesh-Ardakani, R; Rudbari, HA; Munawar, KS; Ashfaq, M; Tahir, MN or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Authors Paul, A; Shipman, MA; Onabule, DY; Sproules, S; Symes, MD in ROYAL SOC CHEMISTRY published article about in [Paul, Avishek; Shipman, Michael A.; Onabule, Dolapo Y.; Sproules, Stephen; Symes, Mark D.] Univ Glasgow, Sch Chem, WestCHEM, Univ Ave, Glasgow G12 8QQ, Lanark, Scotland in 2021, Cited 30. Category: alcohols-buliding-blocks. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

The enhancement of reactivity inside supramolecular coordination cages has many analogies to the mode of action of enzymes, and continues to inspire the design of new catalysts for a range of reactions. However, despite being a near-ubiquitous class of reactions in organic chemistry, enhancement of the reduction of carbonyls to their corresponding alcohols remains very much underexplored in supramolecular coordination cages. Herein, we show that encapsulation of small aromatic aldehydes inside a supramolecular coordination cage allows the reduction of these aldehydes with the mild reducing agent sodium cyanoborohydride to proceed with high selectivity (ketones and esters are not reduced) and in good yields. In the absence of the cage, low pH conditions are essential for any appreciable conversion of the aldehydes to the alcohols. In contrast, the specific microenvironment inside the cage allows this reaction to proceed in bulk solution that is pH-neutral, or even basic. We propose that the cage acts to stabilise the protonated oxocarbenium ion reaction intermediates (enhancing aldehyde reactivity) whilst simultaneously favouring the encapsulation and reduction of smaller aldehydes (which fit more easily inside the cage). Such dual action (enhancement of reactivity and size-selectivity) is reminiscent of the mode of operation of natural enzymes and highlights the tremendous promise of cage architectures as selective catalysts.

Category: alcohols-buliding-blocks. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Paul, A; Shipman, MA; Onabule, DY; Sproules, S; Symes, MD or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Recommanded Product: (4-Methoxyphenyl)methanol. Authors Pandey, VK; Tiwari, CS; Rit, A in AMER CHEMICAL SOC published article about in [Pandey, Vipin K.; Tiwari, Chandra Shekhar; Rit, Arnab] Indian Inst Technol Madras, Dept Chem, Chennai 600036, Tamil Nadu, India in 2021, Cited 56. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5

AgSbF6 was developed as an effective catalyst for the hydroboration of various unsaturated functionalities (nitriles, alkenes, and aldehydes). This atom-economic chemoselective protocol works effectively under low catalyst loading, base- and solvent-free moderate conditions. Importantly, this process shows excellent functional group tolerance and compatibility with structurally and electronically diverse substrates (>50 examples). Mechanistic investigations revealed that the reaction proceeds via a radical pathway. Further, the obtained N,N-diborylamines were showcased to be useful precursors for amide synthesis.

About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Pandey, VK; Tiwari, CS; Rit, A or concate me.. Recommanded Product: (4-Methoxyphenyl)methanol

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts

Computed Properties of C8H10O2. Ou, W; Xiang, XD; Zou, R; Xu, Q; Loh, KP; Su, CL in [Ou, Wei; Xiang, Xudong; Zou, Ru; Su, Chenliang] Shenzhen Univ, Int Collaborat Lab 2D Mat Optoelect Sci & Technol, Engn Technol Res Ctr 2D Mat Informat Funct Device, Inst Microscale Optoelect, Shenzhen 518060, Peoples R China; [Xu, Qing] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou, Zhejiang, Peoples R China; [Loh, Kian Ping] Natl Univ Singapore, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore published Room-Temperature Palladium-Catalyzed Deuterogenolysis of Carbon Oxygen Bonds towards Deuterated Pharmaceuticals in 2021, Cited 50. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5.

Site-specific incorporation of deuterium into drug molecules to study and improve their biological properties is crucial for drug discovery and development. Herein, we describe a palladium-catalyzed room-temperature deuterogenolysis of carbon-oxygen bonds in alcohols and ketones with D-2 balloon for practical synthesis of deuterated pharmaceuticals and chemicals with benzyl-site (sp(3) C-H) D-incorporation. The highlights of this deoxygenative deuteration strategy are mild conditions, broad scope, practicability and high chemoselectivity. To enable the direct use of D2O, electrocatalytic D2O-splitting is adapted to in situ supply D-2 on demand. With this system, the precise incorporation of deuterium in the metabolic position (benzyl-site) of ibuprofen is demonstrated in a sustainable and practical way with D2O.

Computed Properties of C8H10O2. About (4-Methoxyphenyl)methanol, If you have any questions, you can contact Ou, W; Xiang, XD; Zou, R; Xu, Q; Loh, KP; Su, CL or concate me.

Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts