Category: 88-68-6

Dang, MHD; Nguyen, TTM; Nguyen, LHT; Nguyen, TTT; Phan, TB; Tran, PH; Doan, TLH in [Minh-Huy Dinh Dang; Trang Thi Minh Nguyen; Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thang Bach Phan; Tan Le Hoang Doan] Ctr Innovat Mat & Architectures INOMAR, Ho Chi Minh City, Vietnam; [Minh-Huy Dinh Dang; Trang Thi Minh Nguyen; Linh Ho Thuy Nguyen; Trang Thi Thu Nguyen; Thang Bach Phan; Phuong Hoang Tran; Tan Le Hoang Doan] Vietnam Natl Univ Ho Chi Minh City, Ho Chi Minh City, Vietnam; [Phuong Hoang Tran] Univ Sci, Fac Chem, Dept Organ Chem, Ho Chi Minh City, Vietnam published Effect of Fe(iii)-based MOFs on the catalytic efficiency of the tandem cyclooxidative reaction between 2-aminobenzamide and alcohols in 2020, Cited 63. Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

The catalytic properties of metal-organic frameworks (MOFs) containing triangular Fe(iii) clusters in the promotion of organic syntheses and photocatalysis applications have been receiving substantial attention for decades. These clusters are appealing due to the strong Lewis acidity afforded by coordinatively unsaturated sites upon the removal of solvent from the framework. In this paper, triangular Fe(iii) cluster-based MOFs were shown to be highly efficient heterogeneous catalysts for the solvent-free one-pot condensation of 2-aminobenzamide and alcohols to form quinazolin-4-ones under microwave irradiation. The Fe-MOF catalysts ranging from microporous to mesoporous structures with a variety of geometrical pore structures were investigated. Because of the open accessible spaces for reactants and high density of active sites, MOF-907, built from trimer Fe clusters and a mixture of two linkers, was more effective than other Fe(iii)-MOFs. The catalyst can be used for a broad substrate scope and recycled several times without a significant drop-off in its activity.

About 2-Aminobenzamide, If you have any questions, you can contact Dang, MHD; Nguyen, TTM; Nguyen, LHT; Nguyen, TTT; Phan, TB; Tran, PH; Doan, TLH or concate me.. Formula: C7H8N2O

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Torano, JS; Gagarinov, IA; Vos, GM; Broszeit, F; Srivastava, AD; Palmer, M; Langridge, JI; Aizpurua-Olaizola, O; Somovilla, VJ; Boons, GJ in WILEY-V C H VERLAG GMBH published article about RESIDUE LOSS; N-GLYCANS; ROLES in [Torano, Javier Sastre; Gagarinov, Ivan A.; Vos, Gael M.; Broszeit, Frederik; Srivastava, Apoorva D.; Aizpurua-Olaizola, Oier; Somovilla, Victor J.; Boons, Geert-Jan] Univ Utrecht, Dept Chem Biol & Drug Discovery, Univ Weg 99, NL-3584 CG Utrecht, Netherlands; [Palmer, Martin; Langridge, James, I] Waters Corp, Stamford Ave,Altrincham Rd, Wilmslow SK9 4AX, Cheshire, England; [Boons, Geert-Jan] Univ Georgia, Complex Carbohydrate Res Ctr, 315 Riverbend Rd, Athens, GA 30602 USA; [Boons, Geert-Jan] Univ Georgia, Dept Chem, 315 Riverbend Rd, Athens, GA 30602 USA in 2019, Cited 36. Recommanded Product: 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

The fucosylation of glycans leads to diverse structures and is associated with many biological and disease processes. The exact determination of fucoside positions by tandem mass spectrometry (MS/MS) is complicated because rearrangements in the gas phase lead to erroneous structural assignments. Here, we demonstrate that the combined use of ion-mobility MS and well-defined synthetic glycan standards can prevent misinterpretation of MS/MS spectra and incorrect structural assignments of fucosylated glycans. We show that fucosyl residues do not migrate to hydroxyl groups but to acetamido moieties of N-acetylneuraminic acid as well as N-acetylglucosamine residues and nucleophilic sites of an anomeric tag, yielding specific isomeric fragment ions. This mechanistic insight enables the characterization of unique IMS arrival-time distributions of the isomers which can be used to accurately determine fucosyl positions in glycans.

Recommanded Product: 2-Aminobenzamide. Bye, fridends, I hope you can learn more about C7H8N2O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Safety of 2-Aminobenzamide. In 2019 CHEMISTRYSELECT published article about MIXED-METAL OXIDES; OXIDATIVE SYNTHESIS; FACILE; QUINAZOLIN-4(3H)-ONES in [Hase, Dattatraya, V; Jayaram, Radha, V] Inst Chem Technol, Dept Chem, Mumbai 400019, Maharashtra, India; [Thirumalai, Kuppulingam; Swaminathan, Meenakshisundaram] Annamalai Univ, Photocatalysis Lab, Dept Chem, Annamalainagar 608002, Tamil Nadu, India; [Swaminathan, Meenakshisundaram] Kalasalingam Univ, Int Res Ctr, Dept Chem, Nanomat Lab, Krishnan Kovil 626126, Tamil Nadu, India in 2019, Cited 35. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

In the present study, ZnO modified with rare earth oxides GdxMn; M=Mo, V, W) were synthesized by hydrothermal process and their catalytic activity was tested in an oxidative cyclization reaction for the selective synthesis of quinazolinones. The catalysts were characterized by various techniques such as BET surface area analysis, XRD, SEM-EDX, DSC-TGA, ICP-MS and elemental color mapping. 5 wt% Gd2MoO6/ZnO exhibited good catalytic activity and gave 60-91% of Quinazolin-4(3H) ones in toluene. The catalysts could be reused at least four times without loss of catalytic activity.

Safety of 2-Aminobenzamide. Bye, fridends, I hope you can learn more about C7H8N2O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Synthesis and antitumor activities of novel bis-quinazolin-4(3H)-ones WOS:000505757300001 published article about BREAST-CANCER; DERIVATIVES; QUINAZOLINONES; 2-AMINOBENZAMIDES in [Rahmannejadi, Nasrin] Islamic Azad Univ, Dept Chem Sci, Tehran, Iran; [Rahmannejadi, Nasrin] Islamic Azad Univ, Res Branch, Tehran, Iran; [Yavari, Issa] Tarbiat Modares Univ, Dept Chem, POB 14115-175, Tehran, Iran; [Khabnadideh, Soghra] Shiraz Univ Med Sci, Pharmaceut Sci Res Ctr, Shiraz, Iran in 2020, Cited 28. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Name: 2-Aminobenzamide

With the aim of obtaining new antitumor agents, a series of bis-quinazolin-4(3H)-ones (3a-3 f) were designed and synthesized. These products contain 4-oxo-1,2,3,4-tetrahydro-quinazoline and 3H-quinazolin-4-one moieties linked together via a propyl chain. Cytotoxic activities of 3a-3 f were evaluated against lung adenocarcinoma (A549), breast carcinoma (MCF-7) and ovarian cancer (SKOV3) cell lines using MTT method. Cisplatin was used as a positive control. Among the tested compounds 3a, 3b, and 3e showed the best cytotoxic activities against all cancerous cell lines with IC50 values even less than cisplatin. Compounds 3d and 3f also showed desirable cytotoxic activities especially against A549 and MCF-7.

Name: 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Rahmannejadi, N; Yavari, I; Khabnadideh, S or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

In 2020 J INORG ORGANOMET P published article about N-FORMYLATION; FACILE SYNTHESIS; DOPED TIO2; METAL-ION; NANOCOMPOSITE; NANOPARTICLES; FABRICATION; TITANIA; ALDEHYDES; REMOVAL in [Warrier, Vipul G.; Nizam, Aatika] Christ Univ, Dept Chem, Hosur Rd, Bengaluru 560029, India; [Nagaraju, G.] Siddaganga Inst Technol, Dept Chem, Tumakuru 572103, India in 2020, Cited 46. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Product Details of 88-68-6

Facile green synthesis of BiOCl-TiO2 was done using combustion technique by Ixora coccinea leaf extract as fuel source. The said material was characterized using XRD, SEM, EDX, HRTEM, SAED, FTIR, and UV-DRS. The particle size was found to be approximately 60 nm and a crystallite size of 0.3 nm from TEM. The photocatalytic activity of the material was found out using photoluminescence studies, dye degradation and photocatalytic organic conversion. The material showed excellent dye degradation capacity for methylene blue with 80% of the dye degraded under 3 hrs. The stabilisation of electron-hole pair by the heterostructure gave it the ability to perform easy degradation. The degradation kinetics have also been studied. It also showed an excellent organic conversion property with formylation yield reaching up to 96% and total conversion of the reactant molecule. The material is a potent photocatalyst due to its great efficiency and can have a remarkable role in the synthesis of important organic molecules and detoxification of environment.Graphical AbstractThe heterostructure catalyses the conversion of amine to amides and mineralizes methylene blue under visible light condition.

Welcome to talk about 88-68-6, If you have any questions, you can contact Warrier, VG; Nizam, A; Nagaraju, G or send Email.. Product Details of 88-68-6

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Name: 2-Aminobenzamide. Authors Guo, YB; Gao, ZH; Li, JC; Bi, XJ; Shi, EX; Xiao, JH in ROYAL SOC CHEMISTRY published article about in [Guo, Yongbiao; Gao, Zhenhua; Li, Junchen; Bi, Xiaojing; Shi, Enxue; Xiao, Junhua] State Key Lab NBC Protect Civilian, Beijing, Peoples R China in 2021, Cited 30. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Herein, we report on the highly efficient and practical synthesis of 2,3-dihydroquinazolinones directly from diverse aldehydes with excellent yields and enantioselectivity. Particularly, this protocol affords better enantiocontrol for aliphatic aldehydes (up to 99% yield, 97% ee), which always gave unsatisfactory results in the previous studies. Moreover, this catalytic system shows wide tolerance to different functional groups such as alkenyl, nitro and halogens. Most importantly, its practicability is well elucidated via the gram-scale synthesis of different types of products at 0.1 mol% catalyst loading and the simplified work-up procedure. To better understand the reaction pathway and origin of the enantioselectivity, DFT calculations were also performed.

Name: 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Guo, YB; Gao, ZH; Li, JC; Bi, XJ; Shi, EX; Xiao, JH or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

In 2019 CHINESE CHEM LETT published article about BIOLOGICAL-ACTIVITIES; MANNICH-BASES; DESIGN; ANTIFUNGAL; FLUORINE; PRODUCT; ANALOGS in [Chen, Xiulei; Jia, Haowu; Li, Zhong; Xu, Xiaoyong] East China Univ Sci & Technol, Sch Pharm, Shanghai Key Lab Chem Biol, Shanghai 200237, Peoples R China; [Li, Zhong; Xu, Xiaoyong] Shanghai Collaborat Innovat Ctr Biomfg Technol, Shanghai 200237, Peoples R China in 2019, Cited 24. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. COA of Formula: C7H8N2O

To explore new skeleton with nematicidal activity, a series of novel 1,2,3-benzotriazin-4-one derivatives containing piperazine as linker were synthesized and varied fragments were also introduced to increase structure diversity of the new skeleton. Their inhibitory activities in vivo were evaluated against Meloidogyne incognita. The newly prepared compounds A6, A8, A21, A28 and A38 exhibited more than 50% inhibition at the concentration of 20 mg/L. Especially compound A6 displayed 71.4% inhibition against Meloidogyne incognita at the concentration of 20 mg/L. The nematicidal activities varied significantly depending on the types and positions of the substituents, which provided guidance for further structure modification. (C) 2019 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

Welcome to talk about 88-68-6, If you have any questions, you can contact Chen, XL; Jia, HW; Li, Z; Xu, XY or send Email.. COA of Formula: C7H8N2O

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Microwave-Assisted N-Allylation/Homoallylation-RCM Approach: Access to Pyrrole-, Pyridine-, or Azepine-Appended (Het)aryl Aminoamides WOS:000527748400044 published article about OLEFIN METATHESIS; DERIVATIVES; CYCLIZATION; PIPERIDINE in [Novanna, Motakatla; Kannadasan, Sathananthan] Vellore Inst Technol, Sch Adv Sci, Dept Chem, Vellore 632014, Tamil Nadu, India; [Shanmugam, Ponnusamy] CSIR, Organ & Bio Organ Chem Div, Cent Leather Res Inst, Chennai 600020, Tamil Nadu, India in 2020, Cited 38. Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A facile and diversity-oriented approach has been developed for the synthesis of pyrrole-, pyridine-, or azepine-appended (het)aryl aminoamides via the N-allylation/homoallylation-ring-closing metathesis (RCM) strategy. Microwave condition was efficiently utilized for N-allylation of (het)aryl aminoamides to synthesize di-, tri-, and tetra-allyl/homoallylated RCM substrates in good yields. All of the RCM substrates were successfully converted to respective pyrroles 6a-h, 13a,b, 15a,b, pyridines 11a-d, 13c, and azepines 7a,b via RCM. All of the five-, six-, and seven-membered N-heterocycles were synthesized in shorter reaction times with excellent yields without isomerization products. A one-pot reaction to synthesize compounds 6a and 6b without isolating corresponding RCM substrates was achieved successfully. The synthetic utility of the compound 6b has been demonstrated by synthesizing biaryl derivatives 17a,b under the microwave Suzuki coupling reaction condition.

Formula: C7H8N2O. Welcome to talk about 88-68-6, If you have any questions, you can contact Novanna, M; Kannadasan, S; Shanmugam, P or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Design, synthesis and biological activity of selective hCAs inhibitors based on 2-(benzylsulfinyl)benzoic acid scaffold WOS:000480545500001 published article about CARBONIC-ANHYDRASE-IX; FASCINATING MOLECULAR FRAMEWORK; ENANTIOSEPARATION ABILITY; SULFONAMIDE DERIVATIVES; DRUG DISCOVERY; CANCER; PH; 3-(PHENYL-4-OXY)-5-PHENYL-4,5-DIHYDRO-(1H)-PYRAZOLE; ENANTIOMERS; ASSIGNMENT in [Rotondi, Giulia; Guglielmi, Paolo; Secci, Daniela; De Monte, Celeste] Sapienza Univ Rome, Dipartimento Chim & Tecnol Farmaco, Ple A Moro 5, I-00185 Rome, Italy; [Carradori, Simone; De Filippis, Barbara; Maccallini, Cristina; Amoroso, Rosa] G DAnnunzio Univ Chieti Pescara, Dept Pharm, Chieti, Italy; [Cirilli, Roberto] Ist Super Sanita, Ctr Nazl Controllo & Valutaz Farm, Rome, Italy; [Akdemir, Atilla] Bezmialem Vakif Univ, Dept Pharmacol, Fac Pharm, Comp Aided Drug Discovery Lab, Istanbul, Turkey; [Angeli, Andrea; Supuran, Claudiu T.] Univ Firenze, Sect Pharmaceut & Nutraceut Sci, Neurofarba Dept, Via U Schiff 6, I-50019 Florence, Italy in 2019, Cited 48. COA of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A large library of derivatives based on the scaffold of 2-(benzylsulfinyl)benzoic acid were synthesised and tested as atypical inhibitors against four different isoforms of human carbonic anhydrase (hCA I, II, IX and XII, EC 4.2.1.1). The exploration of the chemical space around the main functional groups led to the discovery of selective hCA IX inhibitors in the micromolar/nanomolar range, thus establishing robust structure-activity relationships within this versatile scaffold. HPLC separation of some selected chiral compounds and biological evaluation of the corresponding enantiomers was performed along with molecular modelling studies on the most active derivatives.

COA of Formula: C7H8N2O. Welcome to talk about 88-68-6, If you have any questions, you can contact Rotondi, G; Guglielmi, P; Carradori, S; Secci, D; De Monte, C; De Filippis, B; Maccallini, C; Amoroso, R; Cirilli, R; Akdemir, A; Angeli, A; Supuran, CT or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Name: 2-Aminobenzamide. Authors Thorve, PR; Maji, B in ROYAL SOC CHEMISTRY published article about in [Thorve, Pradip Ramdas; Maji, Biplab] Indian Inst Sci Educ & Res Kolkata, Dept Chem Sci, Mohanpur 741246, India in 2021, Cited 72. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Herein, we report a bioinspired catalytic system for the one-pot cascade oxidation of a native primary amine and an in situ generated non-native secondary amine. The catalyst consists of an o-quinone cofactor phd (1,10-phenanthroline-5,6-dione) and a copper ion and operates under ambient air conditions. Quinazolin-4(3H)-ones, which are common pharmacophores present in numerous pharmaceuticals and bioactive compounds, were synthesized in high yields. A detailed kinetic and mechanistic study elucidates the role of the catalyst in the multi-step oxidative cascade reaction.

Name: 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Thorve, PR; Maji, B or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem