Tag: M.W=100-150

In 2019 RSC ADV published article about DENSITY-FUNCTIONAL THERMOCHEMISTRY; CORROSION INHIBITION PROPERTIES; MILD-STEEL; ABSOLUTE ELECTRONEGATIVITY; CARBON-STEEL; QUINOLINE DERIVATIVES; ELECTRONIC-STRUCTURE; QUANTUM-CHEMISTRY; HARDNESS; ADSORPTION in [Dagdag, Omar; El Harfi, Ahmed] Ibn Tofail Univ, LAPPE, Dept Chem, Fac Sci, BP 133, Kenitra 14000, Morocco; [Cherkaoui, Omar] Higher Sch Text & Clothing Ind, Lab REMTEX, BP 7731, Casablanca, Morocco; [Safi, Zaki] AlAzhar Univ Gaza, Dept Chem, Fac Sci, POB 1277, Gaza, Palestine; [Wazzan, Nuha] King Abdulaziz Univ, Dept Chem, Fac Sci, POB 42805, Jeddah 21589, Saudi Arabia; [Guo, Lei] Tongren Univ, Sch Mat & Chem Engn, Tongren 554300, Peoples R China; [Akpan, E. D.; Verma, Chandrabhan; Ebenso, E. E.] North West Univ, Dept Chem, Fac Nat & Agr Sci, Sch Chem & Phys Sci, Private Bag X2046, ZA-2735 Mmabatho, South Africa; [Akpan, E. D.; Verma, Chandrabhan; Ebenso, E. E.] North West Univ, Mat Sci Innovat & Modelling MaSIM Res Focus Area, Fac Nat & Agr Sci, Private Bag X2046, ZA-2735 Mmabatho, South Africa; [Jalgham, Ramzi T. T.] Bani Walid Univ, Fac Engn, Dept Oil & Gas, Bani Walid, Libya in 2019, Cited 67. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Formula: C7H8N2O

A new epoxy monomer, namely, tetraglycidyl-1,2-aminobenzamide (ER), was synthesized by condensation of the amines with epichlorohydrin in a basic medium. The obtained epoxy monomer was characterized by FT-IR and H-1 NMR spectroscopy. Rheological properties of this monomer were determined using an advanced rheometer. Subsequently, the synthesized ER monomer was investigated as corrosion inhibitor for carbon steel in 1 M HCl solution. The adsorption properties of ER were analyzed by electrochemical, surface investigation and theoretical computational studies using DFT and molecular dynamics (MD). Results showed a high dependence of the viscosity of ER on temperature and concentration, and also, that ER has better inhibition performance. A good agreement between the results derived from computational (MD and DFT) and experimental methods was observed. The thermodynamic parameters, along with the kinetic parameters, showed that the adsorption of ER molecules onto carbon steel surface obeyed the Langmuir isotherm model, and the adsorption at metal-electrolyte interfaces involved both chemical and physical adsorption, but predominantly chemisorption mechanism.

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

An article Synthesis, molecular packing and anti-cholinesterase activity of some new C-2 N-substituted anthranilamide derivatives WOS:000489324100006 published article about 2-AMINOBENZAMIDE DERIVATIVES; BIOLOGICAL EVALUATION; CRYSTAL-STRUCTURES; QUINAZOLINONES; INHIBITORS; EFFICIENT; DESIGN in [Sarfraz, Muhammad; Sultana, Nargis; Tariq, Muhammad Ilyas] Univ Sargodha, Dept Chem, Sargodha 40100, Pakistan; [Parvez, Masood] Univ Calgary, Dept Chem, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada in 2019, Cited 30. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Application In Synthesis of 2-Aminobenzamide

Synthesis of C-2 N-substituted anthranilamide derivatives was carried out in a straight forward manner, utilizing 2-aminobenzamide and benzyl chloride as starting materials. Their crystal structures have been established by single crystal X-ray crystallographic method. In the molecules of 2-benzylamino-benzamide (3a), intramolecular hydrogen bonding b/w O atom and proton of -NH and classical intermolecular hydrogen bonding of the type N-H center dot center dot center dot O forming eight membered rings in R-4(2)(8) pattern. In both molecules of 2-(dibenzylamino)benzamide (3b), unlike the molecule in 3a, each H atoms is pointed towards N atom causing intramolecular hydrogen bonding interactions, resulting in S(6) motifs. However, it is interesting to note that both molecules in 3b are lying about inversion centres and form dimers in R-4(2)(8) motifs; the two dimers are linked via non-classical intermolecular hydrogen bonds C-H center dot center dot center dot O resulting in clusters of four molecules in the structure. In vitro assay results revealed that molecule 3b with IC50 values of 3.8 +/- 0.08 mu M (AChE) and 17.6 +/- 1.10 mu M (BChE) possessed better cholinesterase (AChE and BChE) inhibition potential as compared to standard drug galantamine. Preliminary in silico studies showed that more biological active derivatives were also having good pharmacokinetic profile with no AMES toxicity and carcinogenicity.

Application In Synthesis 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

Name: 2-Aminobenzamide. In 2020 ORG BIOMOL CHEM published article about DIORGANYL DISELENIDES SYNTHESIS; C-H ACTIVATION; ELECTROPHILIC CYCLIZATION; IRON(III) CHLORIDE; BETA-PHENYLETHYLAMINES; CATALYZED ANNULATION; TANDEM CYCLIZATION; BOND FORMATION; DERIVATIVES; 2-ALKYNYLBENZALDEHYDES in [Sonawane, Amol D.; Sonawane, Rohini A.; Win, Khin Myat Noe; Ninomiya, Masayuki; Koketsu, Mamoru] Gifu Univ, Dept Chem & Biomol Sci, Fac Engn, Gifu 5011193, Japan in 2020, Cited 58. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

An efficient, metal free and environment friendly synthesis of isoquinoline-fused benzimidazole has been developed via in situ air oxidation. Also, syntheses of isoquinoline-fused quinazolinone heteroacenes were successfully achieved. The synthesized isoquinoline-fused benzimidazole and isoquinoline-fused quinazolinone derivatives showed lambda(max), F-max and phi(f) values in the ranges 356-394 nm, 403-444 nm and 0.063-0.471, respectively, in CHCl3.

Name: 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Sonawane, AD; Sonawane, RA; Win, KMN; Ninomiya, M; Koketsu, M or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

I found the field of Biochemistry & Molecular Biology; Chemistry; Pharmacology & Pharmacy very interesting. Saw the article Synthesis, crystal structure and antimicrobial activity of 2-((2-(4-(1H-1,2,4-triazol-1-yl)phenyl)quinazolin-4-yl)oxy)-N-phenylacetamide derivatives against phytopathogens published in 2019. HPLC of Formula: C7H8N2O, Reprint Addresses Bao, XP (corresponding author), Guizhou Univ, Ctr Res & Dev Fine Chem, Minist Educ,Key Lab Green Pesticide & Agr Bioengn, State Key Lab Breeding Base Green Pesticide & Agr, Guiyang 550025, Guizhou, Peoples R China.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

A total of eighteen 2-((2-(4-(1H-1,2,4-triazol-1-yl)phenyl)quinazolin-4-yl)oxy)-N-phenylacetamide derivatives were designed and synthesized, via hybrid pharmacophore approach. Among these compounds, chemical structure of compound 4a was unambiguously confirmed by means of single-crystal X-ray diffraction analysis. All the compounds were evaluated in vitro for their inhibition activity against several important phytopathogenic bacteria and fungi in agriculture. The obtained results indicated that several compounds demonstrated potent antibacterial activity against Xanthomonas oryzae pv. oryzae (Xoo). For example, compounds 4c, 4g and 4q had EC50 values of 35.0, 36.5 and 32.4 mu g/mL toward this bacterium, respectively, around 1.5 times more active than commercial bactericide bismerthiazol (EC50 = 89.8 mu g/mL). Additionally, compounds 4j and 4p were found to display comparable antifungal activity against Gloeosporium fructigenum at 50 mu g/mL, to commercial fungicide hymexazol. Finally, the relationships between antibacterial activities and molecular structures of this class of compounds were discussed in detail. [GRAPHICS] .

HPLC of Formula: C7H8N2O. Welcome to talk about 88-68-6, If you have any questions, you can contact Fan, ZJ; Shi, J; Luo, N; Bao, XP or send Email.

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

Recently I am researching about GOLD(I)-CATALYZED CASCADE; METATHESIS REACTION; TANDEM REACTION; CYCLIZATION; EFFICIENT; ALKYNES; HYDROCARBOXYLATION; COMPLEXES; ACCESS, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21472024, 21242008]. Recommanded Product: 88-68-6. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Zheng, YY; Liu, JM; Lei, XS. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

A simple, efficient, and mild method for the preparation of aryl-fused heterocycles has been developed using alpha,omega-alkynoic acids and arylethylamines. In the present method, one of Grubbs’ ruthenium carbenes is able to catalyze the formation of exocyclic enol lactones from alpha,omega-alkynoic acids, which subsequently undergo aminolysis and N-acyl iminium ion formation/cyclization with arylethylamines in the presence of TFA, affording one kind of drug-privileged scaffold. Demonstrated with high functional group tolerance, this new cascade reaction endows the Grubbs’ ruthenium carbene with a new synthetic utility beyond routine olefin metathesis.

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

Quality Control of 2-Aminobenzamide. In 2021 SYNTHETIC COMMUN published article about PRIMARY AMIDES; UREA; DISCOVERY; DERIVATIVES; INHIBITORS; AMINES; TRANSFORMATION; EFFICIENT; KINASE; MAP in [Shamanth, Sadashivamurthy; Sagar, Kunigal S.; Narayana, Yatheesh; Rangappa, Kanchugarakoppal S.; Kempegowda, Mantelingu] Univ Mysore, DOS Chem, Manasagangotri, Mysuru 570006, Karnataka, India; [Nagarakere, Sandhya C.] St Philomenas Coll, PG Dept Studies Chem, Mysuru, India; [Nagarakere, Sandhya C.] St Philomenas Coll, Res Ctr, Mysuru, India; [Mamatha, Mahesha] SRSMN Govt First Grade Coll, Barkur, India in 2021, Cited 38. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Current work describes the environmentally benign approach for the synthesis of o-ureidobenzonitriles, from o-aminobenzamides and isothiocyanates using T3P. Here, the conversion of thiourea to urea and amide to nitrile take place simultaneously via unprecedented intramolecular rearrangement. This protocol is operationally facile and offers wide variety of o-ureidobenzonitriles at room temperature in good to excellent yields.

Quality Control 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

Authors Xie, ZB; Lan, J; Yan, LY; Chen, XH; Li, Q; Meng, J; Le, ZG in ROYAL SOC CHEMISTRY published article about MOLECULAR-OXYGEN; EFFICIENT; 2,3-DIHYDROQUINAZOLIN-4(1H)-ONES; OXIDATION; ALKENES; DERIVATIVES; DESIGN; FACILE; CYCLIZATION; OZONOLYSIS in [Xie, Zongbo; Lan, Jin; Yan, Liyuan; Chen, Xuehua; Li, Qian; Meng, Jia; Le, Zhanggao] East China Univ Technol, Jiangxi Prov Key Lab Synthet Chem, Nanchang 330013, Jiangxi, Peoples R China; [Xie, Zongbo; Lan, Jin; Yan, Liyuan; Chen, Xuehua; Li, Qian; Meng, Jia; Le, Zhanggao] East China Univ Technol, Sch Chem Biol & Mat Sci, Nanchang 330013, Jiangxi, Peoples R China in 2021, Cited 62. Quality Control of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

This is the first report on a facile tandem route for synthesizing quinazolinones at room temperature from various aminobenzamides and in situ-generated aldehydes. The latter was formed via C=C bond cleavage, and the overall reaction proceeded using molecular oxygen as a clean oxidant in the absence of a photocatalyst. Visible light, which was indispensable for the entire course of the reaction, played multiple roles. It initially cleaved styrene to an aldehyde, then facilitated its cyclization with an o-substituted aniline, and finally promoted the dehydrogenation of the cyclized intermediate. The previous step provided the feedstock for the next step in the reaction, thereby preventing volatilization, oxidation, and polymerization of the aldehyde. Thus, the overall process is simple, environmentally benign, and economically feasible.

Welcome to talk about 88-68-6, If you have any questions, you can contact Xie, ZB; Lan, J; Yan, LY; Chen, XH; Li, Q; Meng, J; Le, ZG or send Email.. Quality Control of 2-Aminobenzamide

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

I found the field of Science & Technology – Other Topics very interesting. Saw the article In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox published in 2019. Recommanded Product: 2-Aminobenzamide, Reprint Addresses Sung, B (corresponding author), KIST Europe Forschungsgesell MbH, Saarbrucken, Germany.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

Computational analyses of toxicological processes enables high-throughput screening of chemical substances and prediction of their endpoints in biological systems. In particular, quantitative structure-activity relationship (QSAR) models have been increasingly applied to assess the environmental effects of a plethora of toxic materials. In recent years, some more highlighted types of toxicants are endocrine disruptors (EDs, which are chemicals that can interfere with any hormone-related metabolism). Because EDs may significantly affect animal development and reproduction, rapidly predicting the adverse effects of EDs using in silico techniques is required. This study presents an in silico method to generate prediction data on the effects of representative EDs in aquatic vertebrates, particularly fish species. The protocol describes an example utilizing the automated workflow of the QSAR Toolbox software developed by the Organization for Economic Co-operation and Development (OECD) to enable acute ecotoxicity predictions of EDs. As a result, the following are determined: (1) calculation of the numerical correlations between the concentration for 50% of lethality (LC50) and octanol-water partition coefficient (K-ow), (2) output performances in which the LC50 values determined in experiments are compared to those generated by computations, and (3) the dependence of estrogen receptor binding affinity on the relationship between K-ow and LC50.

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

Recently I am researching about GREEN SYNTHESIS; BIOLOGICAL EVALUATION; ASSISTED SYNTHESIS; EFFICIENT; CATALYST; 2,3-DIHYDROQUINAZOLIN-4(1H)-ONES; QUINAZOLINONES; FACILE, Saw an article supported by the University of Guilan. Published in BENTHAM SCIENCE PUBL LTD in SHARJAH ,Authors: Sina, KF; Yahyazadeh, A; Mahmoodi, NO. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide. Application In Synthesis of 2-Aminobenzamide

2, 3-Dihydroquinazolinones are of popular compounds with the diversification of biological and pharmacological activities. Among many discovered methods, there are efficient and convenient methods used for the synthesis of 2, 3-dihydroquinazoline-4 (1H)-one and some new bis 2, 3-dihydroquinazoline-4 (1H)-one derivatives which are reported in this study. The mentioned methods include the two-component condensation of one molecule of anthranilamide and one molecule of pyrazole carbaldehyde using montmorillonite-K 10 as a catalyst for the preparation of 2, 3 dihydroquinazoline-4 (1H)-ones. Also, one-pot pseudo-five-component reaction (5MCRs) of two molecules of isatoic anhydride, two molecules of pyrazole carbaldehydes and one molecule of ethan-1, 2-diamine in the presence of the r catalyst (montmorillonite-K10) for the synthesis of bis 2, 3-dihydroquinazoline-4 (1H)-ones. Despite the short times of reactions, high yields of products were obtained, which were validated using FT-IR, (HNMR)-H-1, (CNMR)-C-13, and elemental analysis. Moreover, the compounds were screened for their antimicrobial activities against two-gram-positive bacterial strains: Staphylococcus aureus and Micrococcus Luteus; and against two-gram-negative bacterial strains, as well: Escherichia coli and Pseudomonas aeruginosa, which all were utilized for antibacterial investigations. The results showed moderate or significant antibacterial activities.

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

An article Cink4T, a quinazolinone-based dual inhibitor of Cdk4 and tubulin polymerization, identified via ligand-based virtual screening, for efficient anticancer therapy WOS:000459358600010 published article about DEPENDENT KINASE INHIBITOR; MICROTUBULE POLYMERIZATION; CDK4-SPECIFIC INHIBITORS; BIOLOGICAL EVALUATION; SELECTIVE INHIBITORS; CRYSTAL-STRUCTURE; NONPLANAR ANALOG; CYCLIN D1-CDK4; IN-VITRO; PROTEIN in [Sonawane, Vinay; Chaudhuri, Bhabatosh] De Montfort Univ, Leicester Sch Pharm, Leicester LE1 9BH, Leics, England; [Siddique, Mohd Usman Mohd; Sinha, Barij Nayan; Jayaprakash, Venkatesan] Birla Inst Technol, Dept Pharmaceut Sci & Technol, Ranchi 835215, Bihar, India; [Jadav, Surender Singh] Indian Inst Chem Technol, CSIR, Hyderabad 500007, Telangana, India in 2019, Cited 79. Safety of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Inhibition of cyclin dependent kinase 4 (Cdk4) prevents cancer cells from entering the early G(0)/G(1) phase of the cell division cycle whereas inhibiting tubulin polymerization blocks cancer cells’ ability to undergo mitosis (M) late in the cell cycle. We had reported earlier that two non-planar and relatively non-toxic fascaplysin derivatives, an indole and a tryptoline, inhibit Cdk4 with IC50 values of 6.2 and 10 mu M, respectively. Serendipitously, we had also found that they inhibited tubulin polymerization. The molecules were efficacious in mouse tumor models. We have now identified Cink4T in a 59-compound quinazolinone library, designed on the basis of ligand-based virtual screening, as a compound that inhibits Cdk4 and tubulin. Its IC50 value for Cdk4 inhibition is 0.47 mu M and >50 mu M for inhibition of Cdk1, Cdk2, Cdk6, Cdk9. Cink4T inhibits tubulin polymerization with an IC50 of 0.6 mu M. Molecular modelling studies on Cink4T with Cdk4 and tubulin crystal structures lend support to these observations. Cancer cell cycle analyses confirm that Cink4T blocks cells at both G(0)/G(1) and M phases as it should if it were to inhibit both Cdk4 and tubulin polymerization. Our results show, for the very first time, that virtual screening can be used to design novel inhibitors that can potently block two crucial phases of the cell division cycle. (C) 2019 Elsevier Masson SAS. All rights reserved.

Safety of 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Sonawane, V; Siddique, MUM; Jadav, SS; Sinha, BN; Jayaprakash, V; Chaudhuri, B or send Email.

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