Day: November 19, 2021

Recently I am researching about ONE-POT; MULTICOMPONENT REACTIONS; MALONONITRILE DIMER; ACTIVATED NITRILES; DERIVATIVES; CHEMISTRY; REARRANGEMENT; ANTIOXIDANT; REACTIVITY; INHIBITORS, Saw an article supported by the Kuban Science Foundation [MFI-20.1-26/20, MFI-20.1/45]; Ministry of Education and Science of the Russian FederationMinistry of Education and Science, Russian Federation [0795-2020-0031]. Published in MAIK NAUKA/INTERPERIODICA/SPRINGER in NEW YORK ,Authors: Ismiyev, AI; Dotsenko, VV; Aksenov, NA; Aksenova, IV; Magarramov, AM. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde. Category: thiomorpholine

The reaction of aromatic aldehydes with malononitrile, ethyl or butyl cyanoacetate and acetylacetone in the presence of NaOH under mild conditions (EtOH, 25 degrees C) led to the formation of new series of (1S,5R,6R,9R)/(1R,5S,6S,9S)-2-amino-6,9-diaryl-7-acetyl-8-methyl-4-oxo-5-cyano-3-azabicyclo[3.3.1]nona-2,7-diene-1-carboxylic acids esters. A plausible mechanism of the cascade reaction was proposed.

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

Quality Control of 2-Aminobenzamide. Recently I am researching about CATALYZED OXIDATIVE SYNTHESIS; CASCADE SYNTHESIS; O-AMINOBENZAMIDES; N-HETEROCYCLES; LUOTONIN-A; QUINAZOLIN-4(3H)-ONES; DERIVATIVES; CYCLIZATION, Saw an article supported by the CSIRCouncil of Scientific & Industrial Research (CSIR) – India; UGC, New DelhiUniversity Grants Commission, India; DST-INSPIRE, New Delhi. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Ram, S; Shaifali; Chauhan, AS; Sheetal; Sharma, AK; Das, P. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

An efficient and convenient strategy for the synthesis of diversely substituted quinazolinones from o-carbamoyl/cyano aniline and aryl iodides using oxalic acid as a CO source under polystyrene supported palladium (Pd@PS) nanoparticles (NPs) catalyzed conditions has been developed. In this study, oxalic acid has been employed as safe, economic, environmentally benign, sustainable and bench-stable, solid CO surrogate under Double-Layer-Vial (DLV) system for the synthesis of 2-aryl quinazolinones. This methodology does not require any special high-pressure equipment like autoclaves, microwaves, etc. Moreover, a simple procedure for catalyst preparation, catalyst recyclability, easy handling of reaction, additive and base-free generation of CO, excellent to good yields and vast substrate scope are the additional features of developed protocol.

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

Authors Kim, A; Chae, JB; Rha, CJ; Kim, C in WILEY published article about EFFECTIVE CORE POTENTIALS; FLUORESCENT CHEMOSENSOR; MOLECULAR CALCULATIONS; AQUEOUS-SOLUTION; QUANTUM DOTS; CU2+; SENSOR; ZN2+; RECOGNITION; FLUORIDE in [Kim, Ahran; Chae, Ju Byeong; Rha, Chang Joo; Kim, Cheal] Seoul Natl Univ Sci & Technol SNUT, Dept Fine Chem, Seoul 139733, South Korea in 2020, Cited 55. Name: 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A water-applicable hexamethylbenzene (HMB) chemosensor, (E)-2-((2-hydroxy-3-methoxybenzylidene)amino)benzamide, displayed a selective colour change from colourless to yellow in the existence of copper ions. The detection limit was computed as 1.57 mu mol/L, which is substantially lower than the World Health Organisation guideline (31.5 mu mol/L) for copper ions. Probe HMB could also sense and quantify copper ions in real water samples. The coordination mode of HMB to copper ions was demonstrated through Job plot, electrospray ionisation mass spectroscopy and proton nuclear magnetic resonance titration, and was also supported by theoretical studies.

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

Hsiao, YJ; Lin, LY in [Hsiao, Yu-Jui; Lin, Lu-Yin] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei 10608, Taiwan; [Lin, Lu-Yin] Res Ctr Energy Conservat New Generat Residential, Taipei 10608, Taiwan published Enhanced Surface Area, Graphene Quantum Dots, and Functional Groups for the Simple Acid-Treated Carbon Fiber Electrode of Flexible Fiber-Type Solid-State Supercapacitors without Active Materials in 2020.0, Cited 35.0. Recommanded Product: 64-10-8. The Name is 1-Phenylurea. Through research, I have a further understanding and discovery of 64-10-8.

Flexible fiber-type solid-state supercapacitors (FSCs) are demanded for energy storage of wearable soft electronics. A flexible carbon fiber (CF) with high electrical conductivity and good energy storage ability can act as the current collector and the active material simultaneously. Improving the energy storage ability of the CF without depositing active materials is highly promising to avoid active materials from peeling off, especially under bending conditions. In this study, the CF is treated with acid mixtures containing different HNO3 to H2SO4 ratios. The roughened surface and the production of graphene quantum dots and functional groups are achieved for the acid-treated CF, especially for the CF treated with the acid mixtures. The largely enhanced specific capacitance (C-L) is first obtained for the optimized CF electrode (641.08 mF/cm at 5 mV/s) treated with the acid mixture containing the HNO3 to H2SO4 ratio of 1 to 3. The FSC also shows a maximum energy density of 16.57 mu W h/cm at the power density of 62.50 mu W/cm, as well as a C-L retention of 77% and Coulombic efficiency of 100% in 5000 times of a charge/discharge cycling process. Excellent flexibility is also attained for the FSC with no shape distortion of cyclic voltammetry curves measured under the bending angle of 180 degrees and with 1000 times of repeated bending. This work proposes a simple acid treatment to largely enhance the energy storage ability of pure CF electrodes. The bifunctional substance with current collecting and energy storing abilities is expected to be well developed in the future for applying on numerous efficient flexible energy storage devices.

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

Recommanded Product: Anthrone. Authors Richards, C; O’Connor, N; Jose, D; Barrett, A; Regan, F in ROYAL SOC CHEMISTRY published article about in [Richards, Chloe; O’Connor, Nicole; Jose, Diveena; Barrett, Alan; Regan, Fiona] Dublin City Univ, DCU Water Inst, Sch Chem Sci, Dublin 9, Ireland in 2020, Cited 19. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

Biological fouling, also called biofouling, is the undesirable formation of organisms on a surface immersed in water. When the exterior surface of an object such as a vessel is submerged in seawater for a prolonged period, micro and macro organisms usually accumulate on the surface. Biofilms are a set of microorganisms attached to a surface through exopolymers they produce, also known as extracellular polymeric substances (EPS). EPS are a mixture of polymers produced by microorganisms such as bacteria in the presence of biomass. EPS are mainly made up of carbohydrates and proteins, but in smaller quantities, they also contain lipids, nucleic acids, and humic substances. Proteins and carbohydrates found in eps can be quantified by using biochemical methods. The Modified Lowry method, BCA method, and Bradford methods are the common biochemical methods used to quantify protein. Anthrone-sulphuric acid and phenol-sulphuric acid are most common methods used to quantify carbohydrate. The Lowry method was determined to be the best method to quantify protein because it has high precision, low error and low limit of detection. Also, it is highly sensitive and reproducible. The anthrone method was determined to be the best method to quantify carbohydrate because it has high precision, low error, low LOQ. Results were confirmed by testing on substrates deployed in the marine environment to allow establishment of a natural biofilm for study.

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

Zhang, KY; Lu, GL; Xi, ZS; Li, YQ; Luan, QJ; Huang, XB in [Zhang, Kaiyue; Lu, Guilong; Xi, Zuoshuai; Li, Yaqiong; Luan, Qingjie; Huang, Xiubing] Univ Sci & Technol Beijing, Beijing Adv Innovat Ctr Mat Genome Engn, Sch Mat Sci & Engn, Beijing Key Lab Funct Mat Mol & Struct Construct, Beijing 100083, Peoples R China published Covalent organic framework stabilized CdS nanoparticles as efficient visible-light-driven photocatalysts for selective oxidation of aromatic alcohols in 2021, Cited 34. Product Details of 119-61-9. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

Noble-metal-free photocatalysts with high and stable performance provide an environmentally-friendly and cost-efficient route for green organic synthesis. In this work, CdS nanoparticles with small particle size and different amount were successfully deposited on the surface of covalent organic frameworks (COFs). The deposition of suitable content of CdS on COFs could not only modify the light adsorption ability and the intrinsic electronic properties, but also enhance the photocatalytic activity and cycling performance of CdS for the selective oxidation of aromatic alcohols under visible light. Especially, COF/CdS-3 exhibited the highest yield (97.1%) of benzaldehyde which is approximately 2.5 and 15.9 times as that of parental CdS and COF, respectively. The results show that the combination of CdS and COF can improve the utilization of visible light and the separation of photo-generated charge carriers, and COF with the pi-conjugated system as supports for CdS nanoparticles could provide efficient electron transport channels and improve the photocatalytic performance. Therefore, this kind of COF-supported photocatalysts with accelerated photo-induced electrons and charge-carrier separation between semiconductors possesses great potentials in future green organic synthesis. (C) 2021 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.

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

In 2020 RSC ADV published article about ONE-POT SYNTHESIS; HETEROGENEOUS CATALYST; SELECTIVE OXIDATION; C-H; EFFICIENT; DDQ; DERIVATIVES; ALCOHOLS; GREEN; 2-ARYLBENZOTHIAZOLES in [Ghorashi, Nadia; Shokri, Zahra; Moradi, Reza; Rostami, Amin] Univ Kurdistan, Fac Sci, Dept Chem, Sanandaj 6617715175, Iran; [Abdelrasoul, Amira; Rostami, Amin] Univ Saskatchewan, Dept Chem & Biol Engn, 57 Campus Dr, Saskatoon, SK S7N 5A9, Canada in 2020, Cited 53. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Recommanded Product: 88-68-6

The current study applied laccase/DDQ as a bioinspired cooperative catalytic system for the synthesis of quinazolinones (80-95% yield) and benzothiazoles (65-98% yield) using air or O-2 as ideal oxidants in aqueous media at ambient temperature. The aerobic oxidative cyclization reactions occur in two steps: (i) chemical cyclization; (ii) chemoenzymatic oxidation. These methods are more environment-friendly, efficient, simple and practical than other reported methods due to the use of O-2 as an oxidant, laccase as an eco-friendly biocatalyst, aqueous media as the solvent and free from any toxic transition metal and halide catalysts. Therefore, these methods can be applied in pharmaceutical and other sensitive synthetic procedures.

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

An article Glutaconaldehyde as an Alternative Reagent to the Zincke Salt for the Transformation of Primary Amines into Pyridinium Salts WOS:000508468900086 published article about DERIVATIVES; COMPLEXES; IMINES; ENTRY in [Asskar, Ghada; Rivard, Michael; Martens, Thierry] Univ Paris Est, UPEC, CNRS, ICMPE,UMR 7182, F-94320 Thiais, France in 2020, Cited 40. Category: thiomorpholine. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

In the presence of amines, the degradation of glutaconaldehyde in acidic medium can be prevented. By exploitation of this behavior, primary amines are transformed into their corresponding pyridinium salts, including those substrates that remain unreactive toward the Zincke salt, which is the reagent typically used to perform this transformation. The use of glutaconaldehyde also allows control of the nature of the counterion of the pyridinium with no need for additional salt metathesis reaction.

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

Product Details of 119-61-9. Biswal, P; Banjare, SK; Pati, BV; Mohanty, SR; Ravikumar, PC in [Biswal, Pragati; Banjare, Shyam Kumar; Pati, Bedadyuti Vedvyas; Mohanty, Smruti Ranjan; Ravikumar, Ponneri Chandrababu] HBNI, Natl Inst Sci Educ & Res NISER Bhubaneswar, Sch Chem Sci, Khurja 752050, Odisha, India published Rhodium-Catalyzed One-Pot Access to N-Polycyclic Aromatic Hydrocarbons from Aryl Ketones through Triple C-H Bond Activations in 2021.0, Cited 44.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

A Rh-catalyzed pot and step economic synthesis of aza-polycyclic aromatic hydrocarbons (N-PAHs) from readily available aryl ketones and alkynes has been disclosed. Additionally, a novel synthetic application of the well-known aminating reagent hydroxylamine-O-sulfonic acid (HOSA) has been explored as an in situ redox-neutral directing group for the formation of N-PAHs via isoquinoline. Multiple bond formation in a single operation through a cascade of triple C-H bond activations is the beauty of this protocol. The challenging annulations of two different alkynes in a regioselective fashion have been demonstrated effectively. Mechanistic studies reveal that 3,4-diphenyl-1-methylisoquinoline is an active intermediate for this one-pot transformation.

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

Khazanov, TM; Botcha, NK; Yergeshbayeva, S; Shatruk, M; Mukherjee, A in [Khazanov, Thomas M.; Botcha, Niharika Krishna; Mukherjee, Anusree] Univ Alabama, Dept Chem, 301 Sparkman Dr, Huntsville, AL 35899 USA; [Yergeshbayeva, Sandugash; Shatruk, Michael] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA published Investigating reactivity and electronic structure of copper(II)-polypyridyl complexes and hydrogen peroxide in 2021, Cited 88. Safety of Anthrone. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8.

This work presents a detailed study of the reactivity of three mononuclear Cu-II complexes supported by derivatives of the tetradentate ligand N,N’-bis(2-pyridylmethyl)-1,2-ethylenediamine (bispicen). The Cu-II complexes are capable of performing C – H bond activation in the presence of NEt3 and H2O2 through what has been proposed computationally to be a [CuO](+) intermediate. A wavefunction-based quantum chemical investigation into the electronic structure of the proposed [CuO](+) intermediate reveals a triplet ground state predominantly consistent with an S = 1/2 Cu-II center ferromagnetically coupled to an oxyl radical, though contributions from the corresponding biradicaloid CM-oxen resonance structure may be nontrivial. Furthermore, correlation of the electronic structure of the proposed intermediate with analogous high-valent metal-oxo species capable of olefin epoxidation suggests that the Cu-II complexes might be also capable of olefin epoxidation in the presence of NEt3 and H2O2. To test this hypothesis experimentally, the Cu-II complexes are treated with NEt 3 and H2O2 in the presence of alkene substrates, resulting in the formation of epoxides.

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