Month: November 2021

Name: 3-Methylbenzoic acid. 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 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7

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.

Name: 3-Methylbenzoic acid. Welcome to talk about 99-04-7, 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 send Email.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article Mild Liquid Phase Oxidation of Benzyl Alcohol in the Presence of Microporous Framework Copper Silicates WOS:000516846600001 published article about CATALYTIC FAST PYROLYSIS; SELECTIVE OXIDATION; COMPLEXES; ACETONITRILE; BIOMASS in [Neves, Patricia; Valente, Anabela A.; Lin, Zhi] Univ Aveiro, CICECO Aveiro Inst Mat, Dept Chem, P-3810193 Aveiro, Portugal in 2020, Cited 40. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0. Recommanded Product: Benzoic anhydride

The microporous framework copper silicates CuSH-1NaK (1) and SGU-29 (2) – prepared using hydrothermal conditions – are effective heterogeneous oxidation catalysts for producing benzaldehyde (BzAld) and benzoic acid (BzAcid) from benzyl alcohol (BzOH), under mild reaction conditions (approximately atmospheric pressure, 70 degrees C). The copper silicate heterogeneous catalysts triggered a radical reaction mechanism leading to the target products; in particular, BzAcid was formed in up to 94 % yield and 100 % selectivity from BzAld. The type of oxidant and solvent influenced the catalytic performances.

Welcome to talk about 93-97-0, If you have any questions, you can contact Neves, P; Valente, AA; Lin, Z or send Email.. Recommanded Product: Benzoic anhydride

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

Recently I am researching about HETEROBICYCLIC ALKENES; BOND ACTIVATION; AROMATIC KETONES; CARBOXYLIC-ACIDS; BENZOIC-ACIDS; 4+2 ANNULATION; ARYL KETONES; FUNCTIONALIZATION; ARYLATION; PALLADIUM, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21961045, 21572198]; Applied Basic Research Project of Yunnan Province [2017FA004, 2018FB021]; Department of Education of Yunnan Province [2019Y0198]; National Innovation and Entrepreneurship Training Program for College Students; Yunnan Provincial Key Laboratory Construction Plan Funding of Universities. Recommanded Product: 3-Methylbenzoic acid. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Zhang, KY; Khan, R; Chen, JC; Zhang, XX; Gao, Y; Zhou, YY; Li, KK; Tian, YX; Fan, BM. The CAS is 99-04-7. Through research, I have a further understanding and discovery of 3-Methylbenzoic acid

An efficient method for the directing group controlled rhodium-catalyzed addition reaction of oxa/azabicylic alkenes with aromatic ketones and benzoic acids has been developed. The ketones and benzoic acids afforded different addition products when reacted with oxa/azabicyclic alkenes. The reaction between ketones and azabenzonorbornadienes furnished the ring-opening addition products. The reaction between benzoic acids and aza/oxabicyclic alkenes proceeded in the absence of silver salt, giving the 1:2 hydroarylation products in yields up to 96%.

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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

I found the field of Chemistry very interesting. Saw the article Sterically controlled C-H/C-H homocoupling of arenes via C-H borylation published in 2019. Safety of 1,3-Dimethoxybenzene, Reprint Addresses Srinivasan, R (corresponding author), Tianjin Univ, SPST, Bldg 24,92 Weijin Rd, Tianjin 300072, Peoples R China.. The CAS is 151-10-0. Through research, I have a further understanding and discovery of 1,3-Dimethoxybenzene

A mild one-pot protocol for the synthesis of symmetrical biaryls by sequential Ir-catalyzed C-H borylation and Cu-catalyzed homocoupling of arenes is described. The regiochemistry of the biaryl formed is sterically controlled as dictated by the C-H borylation step. The methodology is also successfully extended to heteroarenes. Some of the products obtained by this approach are impossible to obtain via the Ullmann or the Suzuki coupling protocols. Finally, we have shown a one-pot sequence describing C-H borylation/Cu-catalyzed homocoupling/Pd-catalyzed Suzuki coupling to obtain pi-extended arene frameworks.

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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article An Improved N-Acylation of 1 H -Benzotriazole Using 2,2-Dipyridyldisulfide and Triphenylphosphine WOS:000454937600014 published article about FACILE SYNTHESIS; EFFICIENT CONVERSION; ACYLBENZOTRIAZOLES; SULFONES; CLEAVAGE; ESTERS; AMIDES; RING in [Singh, Anoop S.; Agrahari, Anand K.; Mishra, Nidhi; Singh, Mala; Tiwari, Vinod K.] Banaras Hindu Univ, Dept Chem, Inst Sci, Varanasi 221005, Uttar Pradesh, India in 2019, Cited 40. The Name is 2,6-Difluorobenzoic acid. Through research, I have a further understanding and discovery of 385-00-2. Name: 2,6-Difluorobenzoic acid

A novel path has been developed for the conversion of carboxylic acids into the corresponding N -acylbenzotriazoles by using 2,2-dipyridyl disulfide/PPh (3) in anhydrous dichloromethane in the presence of 1 H -benzotriazole. Mild reaction conditions, short reaction time, easy in handling, wide substrate scope, availability of reagents involved, and moreover avoiding the use of base makes this protocol quite useful for the laboratory practices for N -acylbenzotriazole synthesis.

Welcome to talk about 385-00-2, If you have any questions, you can contact Singh, AS; Agrahari, AK; Mishra, N; Singh, M; Tiwari, VK or send Email.. Name: 2,6-Difluorobenzoic acid

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article Synthesis and evaluation of the HIF-1 alpha inhibitory activities of novel ursolic acid tetrazole derivatives WOS:000466365200002 published article about BIOLOGICAL EVALUATION; STRUCTURAL-CHARACTERIZATION; TARGETED THERAPY; ANTICANCER; DESIGN in [Zhang, Lin-Hao; Zhang, Zhi-Hong; Li, Ming-Yue; Jin, Xue-Jun; Piao, Hu-Ri] Yanbian Univ, Key Lab Nat Resources Changbai Mt & Funct Mol, Minist Educ, Coll Pharm, Yanji 133002, Peoples R China; [Wei, Zhi-Yu] Dalian Univ, Coll Med, Dalian 116622, Liaoning, Peoples R China in 2019, Cited 37. Recommanded Product: Benzoic anhydride. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0

The hypoxia-inducible factor-la (HIF-1 alpha) pathway has been implicated in tumor angiogenesis, growth, and metastasis. Therefore, the inhibition of this pathway is an important therapeutic target for the treatment of various types of cancers. Here, we designed and synthesized 31 ursolic acid (UA) derivatives containing a tetrazole moiety and evaluated them for their potential anti-tumor activities as HIF-la transcriptional inhibitors. Of these, compound 14d (IC50 0.8 +/- 0.2 mu M) displayed the most potent activity and compounds 14a (IC50 4.7 +/- 0.2 mu M) exhibited the most promising biological profile. Analysis of the structure-activity relationships of these compounds with HIF-1 alpha suggested that the presence of a tetrazole group located at C-28 of the UA derivatives was critical for their inhibitory activities.

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Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article Redox-neutral photocatalytic strategy for selective C-C bond cleavage of lignin and lignin models via PCET process WOS:000497954900006 published article about PRIMARY ALCOHOL OXIDATION; VISIBLE-LIGHT; ORGANIC FRAMEWORKS; RADICAL CATIONS; CARBON-CARBON; DEPOLYMERIZATION; HYDROGENOLYSIS; TRANSFORMATION; DEGRADATION; BIOMASS in [Wang, Yinling; Liu, Yue; He, Jianghua; Zhang, Yuetao] Jilin Univ, Coll Chem, State Key Lab Supramol Struct & Mat, Changchun 130012, Jilin, Peoples R China in 2019, Cited 62. The Name is 1,3-Dimethoxybenzene. Through research, I have a further understanding and discovery of 151-10-0. Application In Synthesis of 1,3-Dimethoxybenzene

It remains challenging to achieve the selective cleavage of C-C bonds in lignin or lignin model compounds to produce aromatic products in high yield and selectivity. We have developed a redox-neutral photocatalytic strategy to accomplish this goal in both beta-O-4 and beta-1 lignin models at room temperature (RT) via proton-coupled electron transfer (PCET) process without any pretreatments of substrate, by adjusting the alkalinity of base to obtain a lignin models/base PCET pair with a bond dissociation free energy close to 102 kcal/mol. Without breaking down C-beta-C-gamma bond and any C-O bonds, this PCET method is 100% atom economy and produces exclusive C-alpha-C-beta bond cleavage products, such as benzaldehydes (up to 97%) and phenyl ethers (up to 96%), in high to excellent yields and selectivities. Preliminary studies indicated that the PCET strategy is also effective for the depolymerization of native lignin at RT, thus providing significantly important foundation to the depolymerization of lignin. (C) 2019 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.

Welcome to talk about 151-10-0, If you have any questions, you can contact Wang, YL; Liu, Y; He, JH; Zhang, YT or send Email.. Application In Synthesis of 1,3-Dimethoxybenzene

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article Construction of Axial Chirality and Silicon-Stereogenic Center via Rh-Catalyzed Asymmetric Ring-Opening of Silafluorenes WOS:000641296000067 published article about ENANTIOSELECTIVE SYNTHESIS; SILANES; DESYMMETRIZATION; HYDROSILYLATION; DIBENZOSILOLES; ANHYDRIDES; ACTIVATION; ACYLATION; BIARYLS; CARBON in [Bi, Xiufen; Feng, Jia; Xue, Xiaoping; Gu, Zhenhua] Univ Sci & Technol China, Ctr Excellence Mol Synth, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China; [Bi, Xiufen; Feng, Jia; Xue, Xiaoping; Gu, Zhenhua] Univ Sci & Technol China, Ctr Excellence Mol Synth, Dept Chem, Hefei 230026, Anhui, Peoples R China; [Gu, Zhenhua] Minjiang Univ, Ocean Coll, Fuzhou 350108, Fujian, Peoples R China in 2021, Cited 67. The Name is Benzoic anhydride. Through research, I have a further understanding and discovery of 93-97-0. Category: isothiazole

A rhodium-catalyzed enantioselective ring-opening/acylation of silafluorenes is reported. The newly developed bulky phosphoramidite ligand, in combination with methanol as the additive, enabled the reaction to create one axial chirality and one silicon-stereogenic center in a highly selective manner by only cleavage of one Si-C bond.

About Benzoic anhydride, If you have any questions, you can contact Bi, XF; Feng, J; Xue, XP; Gu, ZH or concate me.. Category: isothiazole

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

I found the field of Chemistry; Science & Technology – Other Topics; Materials Science very interesting. Saw the article Surface-Confined Macrocyclization via Dynamic Covalent Chemistry published in 2020. Formula: C8H10O2, Reprint Addresses Zhou, BP (corresponding author), Jinan Univ, Shenzhen Peoples Hosp, Clin Med Coll 2, Ctr Lab,Longhua Branch, Shenzhen 518120, Guangdong, Peoples R China.; Zhou, BP (corresponding author), Jinan Univ, Shenzhen PeoplesH osp, Clin Med Coll 2, Dept Infect Dis, Shenzhen 518120, Guangdong, Peoples R China.; Muccioli, L (corresponding author), Univ Bologna, Dipartimento Chim Ind Toso Montanan, I-40136 Bologna, Italy.; Muccioli, L (corresponding author), Univ Bordeaux, Inst Sci Mol, UMR 5255, F-33405 Talence, France.; Perepichka, DF (corresponding author), McGill Univ, Dept Chem, Montreal, PQ H3A 0B8, Canada.; Orgiu, E (corresponding author), Energie Mat Telecommun Ctr, INRS, Varennes, PQ J3X 1S2, Canada.. The CAS is 151-10-0. Through research, I have a further understanding and discovery of 1,3-Dimethoxybenzene

Surface-confined synthesis is a promising approach to build complex molecular nanostructures including macrocycles. However, despite the recent advances in on-surface macro- cyclization under ultrahigh vacuum, selective synthesis of monodisperse and multicomponent macrocycles remains a challenge. Here, we report on an on-surface formation of [6 + 6] Schiff-base macrocycles via dynamic covalent chemistry. The macrocycles form two-dimensional crystalline domains on the micrometer scale, enabled by dynamic conversion of open-chain oligomers into well-defined similar to 3.0 nm hexagonal macrocycles. We further show that by tailoring the length of the alkyl substituents, it is possible to control which of three possible products-oligomers, macrocycles, or polymers-will form at the surface. In situ scanning tunneling microscopy imaging combined with density functional theory calculations and molecular dynamics simulations unravel the synergistic effect of surface confinement and solvent in leading to preferential on-surface macrocyclization.

Formula: C8H10O2. About 1,3-Dimethoxybenzene, If you have any questions, you can contact Fu, CY; Miksatko, J; Assies, L; Vrkoslav, V; Orlandi, S; Kalbac, M; Kovaricek, P; Zeng, XB; Zhou, BP; Muccioli, L; Perepichka, DF; Orgiu, E or concate me.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com

An article Catalytic C-H aerobic and oxidant-induced oxidation of alkylbenzenes (including toluene derivatives) over VO2+ immobilized on core-shell Fe3O4@SiO2 at room temperature in water WOS:000544674800004 published article about AQUEOUS HYDROGEN-PEROXIDE; SELECTIVE OXIDATION; BOND FUNCTIONALIZATION; SILICA; DEHYDROGENATION; ACID; BENZALDEHYDE; ACTIVATION; OXIDES; METAL in [Mohammadpour, Pegah; Safaei, Elham] Shiraz Univ, Coll Sci, Dept Chem, Shiraz 7194684795, Iran in 2020.0, Cited 78.0. The Name is 3-Methylbenzoic acid. Through research, I have a further understanding and discovery of 99-04-7. Product Details of 99-04-7

Direct C-H bond oxidation of organic materials, and producing the necessary oxygenated compounds under mild conditions, has attracted increasing interest. The selective oxidation of various alkylbenzenes was carried out by means of a new catalyst containing VO2+ species supported on silica-coated Fe3O4 nanoparticles usingt-butyl hydroperoxide as an oxidant at room temperature in H2O or solvent-free media. The chemical and structural characterization of the catalyst using several methods such as FTIR spectroscopy, XRD, FETEM, FESEM, SAED, EDX and XPS showed that VO2+ is covalently bonded to the silica surface. High selectivity and excellent conversion of various toluene derivatives, with less reactive aliphatic (sp(3)) C-H bonds, to related benzoic acids were quite noticeable. The aerobic oxygenation reaction of these alkylbenzenes was studied under the same conditions. All the results accompanied by sustainability of the inexpensive and simple magnetically separable heterogeneous catalyst proved the important criteria for commercial applications.

Product Details of 99-04-7. Welcome to talk about 99-04-7, If you have any questions, you can contact Mohammadpour, P; Safaei, E or send Email.

Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com