Category: 88-68-6

An article Iridium(III)-Catalyzed Alkynylation of 2-(Hetero)arylquinazolin-4-one Scaffolds via C-H Bond Activation WOS:000460491600052 published article about CROSS-COUPLING REACTION; TERMINAL ALKYNES; ETHYNYL BENZIODOXOLONES; CATALYZED ALKYNYLATION; SONOGASHIRA REACTIONS; ARENES; QUINAZOLINONE; AMIDATION; ACETYLENE; AMINATION in [Rohokale, Rajendra S.; Kalshetti, Rupali G.; Ramana, Chepuri V.] CSIR Natl Chem Lab, Div Organ Chem, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India; [Kalshetti, Rupali G.; Ramana, Chepuri V.] Acad Sci & Innovat Res, New Delhi 110025, India in 2019, Cited 80. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Computed Properties of C7H8N2O

The directed C-H alkynylation of 2-(hetero)arylquinazolin-4-ones has been explored with the ethynylbenziodoxolone reagent TIPS-EBX employing an Ir(III) catalyst. Complementary conditions for either monoalkynylation or dialkynylation have been developed. Also demonstrated is the broad scope of this reaction and the compatibility of various functional groups such as -F, -Cl, -Br, -CF3, -OMe, -NO2, and alkyl, etc.

Computed Properties of C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Rohokale, RS; Kalshetti, RG; Ramana, CV or concate me.

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

Application In Synthesis of 2-Aminobenzamide. 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.

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.. Application In Synthesis of 2-Aminobenzamide

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

Erfan, MA; Akhlaghinia, B; Ghodsinia, SSE in [Erfan, Mohammad Anwar; Akhlaghinia, Batool; Ghodsinia, Sara S. E.] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad 9177948974, Razavi Khorasan, Iran published An Efficient Green Protocol for Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones Using SBA-16/GPTMS-TSC-Cu-I under Solvent-Free Conditions in 2020, Cited 87. Product Details of 88-68-6. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Herein a rapid, efficient, facile and environmentally benign synthesis of 2,3-dihydroquinazolin-4(1H)-ones using SBA-16/GPTMS-TSC-Cu-I (Cu-I anchored onto mesoporous SBA-16 functionalized by aminated 3-glycidyloxypropyltrimethoxysilane with thiosemicarbazid) is reported. The aforesaid mesostructured catalyst with a unique super-cage structure and narrow particle size distribution (3-7 nm) exhibited excellent catalytic activity in high yielding preparation of 2,3 dihydroquinazolin-4(1H)-ones from the condensation of 2-aminobenzamide and an aldehyde in solvent-free conditions. Furthermore, SBA-16/GPTMS-TSC-Cu-I as a heterogeneous catalyst was stable under reaction conditions and can be recycled at least five times without any loss of its catalytic efficiency.

Product Details of 88-68-6. About 2-Aminobenzamide, If you have any questions, you can contact Erfan, MA; Akhlaghinia, B; Ghodsinia, SSE or concate me.

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

I found the field of Chemistry very interesting. Saw the article Mukaiyama’s reagent promoted mild protocol for one-pot metal-free synthesis of dihydro quinazolinones published in 2021. Product Details of 88-68-6, Reprint Addresses Rajput, CS (corresponding author), Jubilant Biosys Ltd, B-34,Sect 58, Noida 201301, UP, India.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

We have developed a fast and convenient method to prepare dihydroquinazolin-4(1H)-ones from anthranilamide and different aromatic aldehydes by using the Mukaiyama reagent. The reactions proceeded smoothly with a broad scope of substrates providing the expected products in good to excellent yields under with a low environmental factor and high atom economy. The metal-free condition and the ease of product isolation are the highlighted advantages in solving the issue of trace metal contamination in synthesized pharmaceuticals. (C) 2021 Elsevier Ltd. All rights reserved.

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.. Product Details of 88-68-6

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

Quality Control of 2-Aminobenzamide. In 2019 J ENZYM INHIB MED CH 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. 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.

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.. Quality Control of 2-Aminobenzamide

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

I found the field of Chemistry very interesting. Saw the article Supramolecular Fe3O4@PEG/-diaza crown ether@Ni: a novel magnetically reusable nano catalyst for the clean synthesis of 2-aryl-2,3-dihydroquinazolin-4(1H)-ones published in 2019. Product Details of 88-68-6, Reprint Addresses Pesyan, NN (corresponding author), Urmia Univ, Dept Organ Chem, Fac Chem, Orumiyeh 57159, Iran.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

Ni@diaza crown ether complex supported on magnetic nanoparticle was provided by grafting technique. The catalytic activity of Fe3O4@diaza crown ether@Ni was explored through one-pot synthesis of 2,3-dihydroquinazolin-4(1H)-ones and it was used as an efficient and recoverably constant nanocatalyst. FT-IR, SEM, TEM, XRD, BET, ICP, EDS, and TGA techniques were employed to specify the nanocatalyst. This heterogeneous catalyst demonstrated acceptable recyclability and could be used again several times with no considerable loss of its catalytic activity.

Product Details of 88-68-6. 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

Recently I am researching about SELECTIVE AEROBIC OXIDATION; OXYGEN REDUCTION; COBALT NANOPARTICLES; NITROGEN-HETEROCYCLES; NONPRECIOUS METAL; CASCADE SYNTHESIS; GENERAL-SYNTHESIS; CARBON NANOTUBES; ACTIVE-SITES; C CATALYST, Saw an article supported by the Key Technology R&D Program of Shandong Province [2019GGX102075]; 13th-Five Key Project of the Chinese Academy of Sciences [Y7720519KL]; Royal Society (UK)Royal Society of London [NAF-R2-180695]. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Ma, ZM; Song, T; Yuan, YZ; Yang, Y. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide. COA of Formula: C7H8N2O

In this paper, we developed a reusable heterogeneous non-precious iron nanocomposite comprising metallic Fe-Fe3C nanoparticles and Fe-N-x sites on N-doped porous carbon, which allows for highly efficient synthesis of quinolines and quinazolinones via oxidative coupling of amines and aldehydes using H2O2 as the oxidant in aqueous solution under mild conditions. A set of quinazolines and quinazolinones were synthesized in high yields with a broad substrate scope and good tolerance of functional groups. Characterization and control experiments disclose that a synergistic effect between the metallic Fe nanoparticles and built-in Fe-N-x sites is primarily responsible for the outstanding catalytic performance. Furthermore, the iron nanocomposite could be readily recovered for successive use without appreciable loss in catalytic activity and selectivity. This work provides an expedient and sustainable method to access pharmaceutically relevant N-heterocycles.

Welcome to talk about 88-68-6, If you have any questions, you can contact Ma, ZM; Song, T; Yuan, YZ; Yang, Y or send Email.. COA of Formula: C7H8N2O

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

An article An Efficient Green Protocol for Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones Using SBA-16/GPTMS-TSC-Cu-I under Solvent-Free Conditions WOS:000514728300028 published article about 2-AMINOETHYL DIHYDROGEN PHOSPHATE; ONE-POT SYNTHESIS; MAGNETICALLY REUSABLE NANOCATALYST; HIGHLY ENANTIOSELECTIVE SYNTHESIS; SOLID ACID; 3-COMPONENT SYNTHESIS; HETEROGENEOUS CATALYST; RAPID SYNTHESIS; SUZUKI-MIYAURA; IONIC LIQUID in [Erfan, Mohammad Anwar; Akhlaghinia, Batool; Ghodsinia, Sara S. E.] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad 9177948974, Razavi Khorasan, Iran in 2020, Cited 87. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. SDS of cas: 88-68-6

Herein a rapid, efficient, facile and environmentally benign synthesis of 2,3-dihydroquinazolin-4(1H)-ones using SBA-16/GPTMS-TSC-Cu-I (Cu-I anchored onto mesoporous SBA-16 functionalized by aminated 3-glycidyloxypropyltrimethoxysilane with thiosemicarbazid) is reported. The aforesaid mesostructured catalyst with a unique super-cage structure and narrow particle size distribution (3-7 nm) exhibited excellent catalytic activity in high yielding preparation of 2,3 dihydroquinazolin-4(1H)-ones from the condensation of 2-aminobenzamide and an aldehyde in solvent-free conditions. Furthermore, SBA-16/GPTMS-TSC-Cu-I as a heterogeneous catalyst was stable under reaction conditions and can be recycled at least five times without any loss of its catalytic efficiency.

Welcome to talk about 88-68-6, If you have any questions, you can contact Erfan, MA; Akhlaghinia, B; Ghodsinia, SSE or send Email.. SDS of cas: 88-68-6

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

An article An Efficient Green Protocol for Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones Using SBA-16/GPTMS-TSC-Cu-I under Solvent-Free Conditions WOS:000514728300028 published article about 2-AMINOETHYL DIHYDROGEN PHOSPHATE; ONE-POT SYNTHESIS; MAGNETICALLY REUSABLE NANOCATALYST; HIGHLY ENANTIOSELECTIVE SYNTHESIS; SOLID ACID; 3-COMPONENT SYNTHESIS; HETEROGENEOUS CATALYST; RAPID SYNTHESIS; SUZUKI-MIYAURA; IONIC LIQUID in [Erfan, Mohammad Anwar; Akhlaghinia, Batool; Ghodsinia, Sara S. E.] Ferdowsi Univ Mashhad, Fac Sci, Dept Chem, Mashhad 9177948974, Razavi Khorasan, Iran in 2020, Cited 87. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6. Category: thiomorpholine

Herein a rapid, efficient, facile and environmentally benign synthesis of 2,3-dihydroquinazolin-4(1H)-ones using SBA-16/GPTMS-TSC-Cu-I (Cu-I anchored onto mesoporous SBA-16 functionalized by aminated 3-glycidyloxypropyltrimethoxysilane with thiosemicarbazid) is reported. The aforesaid mesostructured catalyst with a unique super-cage structure and narrow particle size distribution (3-7 nm) exhibited excellent catalytic activity in high yielding preparation of 2,3 dihydroquinazolin-4(1H)-ones from the condensation of 2-aminobenzamide and an aldehyde in solvent-free conditions. Furthermore, SBA-16/GPTMS-TSC-Cu-I as a heterogeneous catalyst was stable under reaction conditions and can be recycled at least five times without any loss of its catalytic efficiency.

Category: thiomorpholine. Welcome to talk about 88-68-6, If you have any questions, you can contact Erfan, MA; Akhlaghinia, B; Ghodsinia, SSE or send Email.

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

I found the field of Chemistry very interesting. Saw the article T3P mediated intramolecular rearrangement of o-aminobenzamide to o-ureidobenzonitrile using isothiocyanates published in 2021. Quality Control of 2-Aminobenzamide, Reprint Addresses Rangappa, KS; Kempegowda, M (corresponding author), Univ Mysore, DOS Chem, Manasagangotri, Mysuru 570006, Karnataka, India.. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

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