Category: 88-68-6

I found the field of Chemistry very interesting. Saw the article Polystyrene-Supported Palladium (Pd@PS)-Catalyzed Carbonylative Annulation of Aryl Iodides Using Oxalic Acid as a Sustainable CO Source for the Synthesis of 2-Aryl Quinazolinones published in 2019. Application In Synthesis of 2-Aminobenzamide, Reprint Addresses Das, P (corresponding author), CSIR Inst Himalayan Bioresource Technol, Nat Prod Chem & Proc Dev Div, Palampur 176061, Himachal Prades, India.; Das, P (corresponding author), CSIR IHBT, Acad Sci & Innovat Res, Palampur 176061, Himachal Prades, India.. 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.

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Ram, S; Shaifali; Chauhan, AS; Sheetal; Sharma, AK; Das, P or concate me.

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

In 2020 SCI REP-UK published article about NANOFIBERS; ARCHITECTURE; TRANSITION; NANOTUBES; GELATORS; NETWORKS; DESIGN; WATER in [Aldilla, Vina R.; Chen, Renxun; Black, David StC; Thordarson, Pall; Kumar, Naresh] Sch Chem, UNSW Sydney NSW, Sydney, NSW 2052, Australia; [Martin, Adam D.] Macquarie Univ, Fac Med & Hlth Sci, Dementia Res Ctr, Sydney, NSW 2109, Australia; [Marjo, Christopher E.; Rich, Anne M.] UNSW Sydney, Mark Wainwright Analyt Ctr, Sydney, NSW 2052, Australia in 2020, Cited 79. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Category: thiomorpholine

In this study, we describe the synthesis and molecular properties of anthranilamide-based short peptides which were synthesised via ring opening of isatoic anhydride in excellent yields. These short peptides were incorporated as low molecular weight gelators (LMWG), bola amphiphile, and C-3-symmetric molecules to form hydrogels in low concentrations (0.07-0.30% (w/v)). The critical gel concentration (CGC), viscoelastic properties, secondary structure, and fibre morphology of these short peptides were influenced by the aromaticity of the capping group or by the presence of electronegative substituent (namely fluoro) and hydrophobic substituent (such as methyl) in the short peptides. In addition, the hydrogels showed antibacterial activity against S. aureus 38 and moderate toxicity against HEK cells in vitro.

Category: thiomorpholine. About 2-Aminobenzamide, If you have any questions, you can contact Aldilla, VR; Chen, RX; Martin, AD; Marjo, CE; Rich, AM; Black, DS; Thordarson, P; Kumar, N or concate me.

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

Safety of 2-Aminobenzamide. In 2020 NEW J CHEM published article about GREEN; NANOPARTICLES; CATALYST; OXIDATION; COMPLEX; ACID; DEGRADATION; SULFIDES; SURFACE; MCM-41 in [Tamoradi, Taiebeh] Islamic Azad Univ, Dept Chem, Izeh, Iran; [Mousavi, Seyedeh Masoumeh] Univ Tehran, Dept Environm Planning, Tehran, Iran; [Mohammadi, Masoud] Ilam Univ, Fac Sci, Dept Chem, Ilam, Iran in 2020, Cited 46. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

In the present study, a facile technique to immobilize praseodymium(iii) complex on the surface of magnetic nanoparticles by using available materials is reported. The prepared samples were characterized by chemical and physical methods such as FTIR, SEM, XRD and EDX and were tested in the synthesis of polyhydroquinoline and 2,3-dihydroquinazolin-4(1H)-one derivatives. It was observed that the yields of the reactions in the presence of the prepared nanocatalyst were good to excellent. More importantly, the use of a recoverable and novel magnetic nanocatalyst in these reactions is the outstanding feature of this protocol.

Safety of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Tamoradi, T; Mousavi, SM; Mohammadi, M or concate me.

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

Recently I am researching about EFFICIENT, Saw an article supported by the SERB New DelhiDepartment of Science & Technology (India)Science Engineering Research Board (SERB), India [EMR/2014/000542]; Jadavpur University, KolkataJadavpur University. Published in INDIAN ACAD SCIENCES in BANGALORE ,Authors: Mondal, MA; Mondal, S; Khan, AA. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide. Category: thiomorpholine

One-pot synthesis of isoindole fused quinazolin 4-ones via intramolecular 1,3 hydride transfer in the presence of acid catalyst has been described. Substrate scope and mechanistic insights were investigated. Substituents on the amide side have a negligible influence on the key step and therefore the method have wide scope for accessing various bicyclic core structure.

Category: thiomorpholine. About 2-Aminobenzamide, If you have any questions, you can contact Mondal, MA; Mondal, S; Khan, AA or concate me.

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

An article Electrostatically Enhanced Sulfuric Acid: A Strong BrOnsted Acidic Catalyst for Multi-Component Reactions WOS:000468172400019 published article about ONE-POT SYNTHESIS; BIGINELLI REACTION; EFFICIENT SYNTHESIS; SOLID ACID; ACTIVATION; LIQUID in [Anzabi, Mohadese Yaghoobi; Yazdani, Hossein; Bazgir, Ayoob] Shahid Beheshti Univ, Dept Chem, GC, Tehran 1983963113, Iran in 2019, Cited 35. SDS of cas: 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

A new electrostatically enhanced sulfuric acid as a strong BrOnsted acidic catalyst has been developed for multi-component reactions. A positively charged center in the catalyst electrostatically activates it for acid-catalyzed multi-component reactions and afforded desired products in short reaction time and near room temperature in EtOH as a green solvent. [GRAPHICS] .

SDS of cas: 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Anzabi, MY; Yazdani, H; Bazgir, A or concate me.

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

Wei, XW; Yuan, JM; Huang, WY; Chen, NY; Li, XJ; Pan, CX; Mo, DL; Su, GF in [Wei, Xin-Wei; Yuan, Jing-Mei; Chen, Nan-Ying; Li, Xiao-Juan; Pan, Cheng-Xue; Mo, Dong-Liang; Su, Gui-Fa] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China; [Huang, Wan-Yun] Guilin Med Univ, Dept Pharmacol, Guilin 541004, Peoples R China published 2-Styryl-4-aminoquinazoline derivatives as potent DNA-cleavage, p53-activation and in vivo effective anticancer agents in 2020, Cited 39. COA of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Forty-eight analogues of CP-31398, an antitumor agent modulated the mutant p53 gene were synthesized and their cytotoxicities against four cancer cell lines with different p-53 status including bladder cell 724 (w-p53), gastric cell MGC-803 (m-p53), prostate cell DU145 (m-p53), prostate cell PC-3 (null-p53), lung cell A549 (w-p53) and normal liver cell line HL-7702 (w-p53) were examined. (E)-2-(4-Nitrostyryl)-4-(3-dimethylaminopropyl)-aminoquinazoline (10ah) was identified as the most potent compound in anti-proliferation against MGC-803 cells, with IC50 lowed to 1.73 mu M, far potency than that of CP-31398. Molecular mechanism study revealed that 10ah and CP-31398 differ greatly in mechanism to exert their antitumor properties. 10ah could intercalate into DNA and resulted in significant DNA double-strand break 10ah-treatment in MGC-803 cells increased the expression of p53, phosphorylated p53 (p-p53), CDK4, p21 to cause cell cycle arrest at G2/M phase, significantly up-regulated the levels of pro-apoptosis proteins Bak, Bax, Bim while down-regulated the anti-apoptosis proteins Bcl-2, Bcl-xL and the levels of cyclin B1, fluctuated the intracellular reactive oxygen species (ROS), Ca2+ and mitochondria! membrane potential, activated Caspase-9 and Caspase-3 to induce apoptosis. 10ah also displayed potent anticancer efficiency against MGC-803 xenograft tumors models, with tumor growth inhibition (TGI) up to 61.8% at 20 mg/kg without obvious toxicity. (C) 2019 Elsevier Masson SAS. All rights reserved.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Wei, XW; Yuan, JM; Huang, WY; Chen, NY; Li, XJ; Pan, CX; Mo, DL; Su, GF or concate me.

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

Li, WL; Yin, Y; Shuai, W; Xu, FJ; Yao, H; Liu, J; Cheng, KG; Xu, JY; Zhu, ZY; Xu, ST in [Li, Wenlong; Yin, Ying; Shuai, Wen; Xu, Feijie; Yao, Hong; Xu, Jinyi; Xu, Shengtao] China Pharmaceut Univ, State Key Lab Nat Med, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China; [Li, Wenlong; Yin, Ying; Shuai, Wen; Xu, Feijie; Yao, Hong; Xu, Jinyi; Xu, Shengtao] China Pharmaceut Univ, Dept Med Chem, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China; [Liu, Jie] China Pharmaceut Univ, Dept Organ Chem, 24 Tong Jia Xiang, Nanjing 210009, Jiangsu, Peoples R China; [Liu, Jie; Cheng, Keguang] Guangxi Normal Univ, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China; [Liu, Jie; Cheng, Keguang] Guangxi Normal Univ, Sch Chem & Pharm, Guilin 541004, Peoples R China; [Zhu, Zheying] Univ Nottingham, Sch Pharm, Div Mol Therapeut & Formulat, Univ Pk Campus, Nottingham NG7 2RD, England published Discovery of novel quinazolines as potential anti-tubulin agents occupying three zones of colchicine domain in 2019, Cited 26. COA of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

A series of novel quinazolines as tubulin inhibitors occupying three zones of colchicine domain have been designed and synthesized inspired by the recently disclosed crystal structure of verubulin analogue 6 with tubulin. Among the newly synthesized compounds, 19c showed noteworthy potency against K562, HepG2, KB, HCT-8 and MDB-MB-231 cancer cells. In vitro microtubule polymerization assays identified 19c as a potent tubulin assembly inhibitor, the binding mode of which with tubulin was confirmed by molecular modeling studies to occupy three zones of tubulin domain. Furthermore, 19c disrupted the intracellular microtubule network, caused G2/M phase arrest, induced cell apoptosis and depolarized mitochondria of K562 cells. 19c also reduced the cell migration and disrupted the capillary-like tube formation of human umbilical vein endothelial cells (HUVECs). Importantly, 19c significantly and dose dependently inhibited tumor growth in H22 liver cancer xenograft mouse model. All these results suggested that 19c deserves further research as a novel and potential anti-tubulin agent for the treatment of cancers.

COA of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Li, WL; Yin, Y; Shuai, W; Xu, FJ; Yao, H; Liu, J; Cheng, KG; Xu, JY; Zhu, ZY; Xu, ST or concate me.

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

An article Highly Efficient Photocatalytic Conversion of Amine to Amide and Degradation of Methylene Blue Using BiOCl-TiO2 Nano Heterostructures WOS:000516034400001 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. HPLC of Formula: C7H8N2O. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery 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.

HPLC of Formula: C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Warrier, VG; Nizam, A; Nagaraju, G or concate me.

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

Recently I am researching about GAMMA-AMINO-ALCOHOLS; NON-INNOCENT LIGANDS; ONE-POT SYNTHESIS; OXIDATIVE SYNTHESIS; O-AMINOBENZAMIDES; RUTHENIUM; KETONES; CYCLIZATION; SECONDARY; QUINAZOLINONES, Saw an article supported by the DSTDepartment of Science & Technology (India) [YSS/2015/001552]; UGCUniversity Grants Commission, India; CSIRCouncil of Scientific & Industrial Research (CSIR) – India; IIESTS; CICECO-Aveiro Institute of Materials [POCI-01-0145-FEDER-007679, UID/CTM/50011/2013]; national funds through the FCT/MEC; FEDEREuropean Commission. Computed Properties of C7H8N2O. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Das, S; Sinha, S; Samanta, D; Mondal, R; Chakraborty, G; Brandao, P; Paul, ND. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

A simple metal-ligand cooperative approach for the dehydrogenative functionalization of alcohols to various substituted quinolines and quinazolin-4(3H)-ones under relatively mild reaction conditions (<= 90 degrees C) is reported. Simple and easy-to-prepare air-stable Cu(II) complexes featuring redox-active azo-aromatic scaffolds, 2-arylazo-(1,10-phenanthroline) (L-1,L-2), are used as catalyst. A wide variety of substituted quinolines and quinazolin-4(3H)-ones were synthesized in moderate to good isolated yields via dehydrogenative coupling reactions of various inexpensive and easily available starting materials under aerobic conditions. A few control experiments and deuterium labeling studies were carried out to understand the mechanism of the dehydrogenative coupling reactions, which indicate that both copper and the coordinated azo-aromatic ligand participate in a cooperative manner during the catalytic cycle. About 2-Aminobenzamide, If you have any questions, you can contact Das, S; Sinha, S; Samanta, D; Mondal, R; Chakraborty, G; Brandao, P; Paul, ND or concate me.. Computed Properties of C7H8N2O

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

Balaji, S; Balamurugan, G; Ramesh, R; Semeril, D in [Balaji, Sundarraman; Balamurugan, Gunasekaran; Ramesh, Rengan] Bharathidasan Univ, Ctr Organometall Chem, Sch Chem, Tiruchirappalli 620024, Tamil Nadu, India; [Semeril, David] Univ Strasbourg, Inst Chim, Lab Chim Inorgan & Catalyse, UMR 7177,CNRS, F-67070 Strasbourg, France published Palladium(II) N boolean AND O Chelating Complexes Catalyzed One-Pot Approach for Synthesis of Quinazolin-4(3H)-ones via Acceptorless Dehydrogenative Coupling of Benzyl Alcohols and 2-Aminobenzamide in 2021, Cited 78. Application In Synthesis of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

A convenient protocol for the one-pot synthesis of quinazolin-4(3H)-ones using palladium(II) complexes via dehydrogenative coupling of readily available benzyl alcohols and 2-aminobenzamide has been described. New structurally related Pd(II) N boolean AND O chelating complexes of general configuration [Pd(L)Cl(PPh3)] (where L = dimethylamino benzoylhydrazone ligands) have been designed and synthesized. The formation of the complexes has been recognized by analytical and spectral methods (FT-IR, NMR, HR-MS). The presence of a square-planar geometry around the palladium(II) ion was confirmed by single crystal X-ray diffraction study. A wide range of substituted quinazolinones have been successfully achieved from a diverse range of benzyl alcohols in good to excellent yields using 1.0 mol % of catalyst loading under aerobic conditions. Furthermore, control experiments reveal that the dehydrogenative coupling reaction involves initially the formation of an aldehyde intermediate and subsequent formation of a cyclic aminal intermediate.

Application In Synthesis of 2-Aminobenzamide. About 2-Aminobenzamide, If you have any questions, you can contact Balaji, S; Balamurugan, G; Ramesh, R; Semeril, D or concate me.

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