Tag: M.W=150-200

An article Bioactive naphthoquinone and anthrone derivatives from endophytic Micromonospora sp. NEAU-gq13 WOS:000500123000002 published article about FUNGI in [Li, Jian-Song; Zhang, Hui; Qi, Huan; Wang, Ji-Dong] Zhejiang Hisun Pharmaceut Co Ltd, Zhejiang Key Lab Antifungal Drugs, Taizhou 318000, Peoples R China; [Xiang, Wen-Sheng] Northeast Agr Univ, Sch Life Sci, Life Sci & Biotechnol Res Ctr, Harbin 150030, Heilongjiang, Peoples R China in 2019, Cited 16. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8. Quality Control of Anthrone

Two new naphthalenone derivatives, 5-hydroxy-4-oxo-2-(2-oxopropyl)-1,2,3,4-tetrahydronaphthalen-1-yl acetate (1) and 5-hydroxy-2-(2-hydroxypropyl)naphthalene-1,4-dione (2), together with two new anthrone derivatives, (S)-2,5-dihydroxy-2-methyl-1,2,3,4-tetrahydroanthracene-9,10-dione (3) and 4,5-dihydroxy-2-methyl-9H-xanthen-9-one (4), were isolated from the fermentation broth of endophytic Micromonospora sp. NEAU-gq13. Their structures were determined by 1D-NMR, 2D-NMR, and HR-ESI-MS analysis. Compounds 2 and 3 exhibited strong cytotoxic activity against human central nervous system cancer (SF-268) with the IC50 values of 3.04 and 5.66 mu g/ml, respectively. Moreover, compound 2 also displayed potent activity against human liver cancer (HepG2) with an IC50 value of 1.01 mu g/ml.

Quality Control of Anthrone. Welcome to talk about 90-44-8, If you have any questions, you can contact Li, JS; Zhang, H; Qi, H; Wang, JD; Xiang, WS or send Email.

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

COA of Formula: C7H5NO3. Authors Liu, CX; Cui, J; Wang, YF; Zhang, MJ in ROYAL SOC CHEMISTRY published article about in [Liu, Chengxin; Zhang, Mingjie] Tianjin Univ, Sch Sci, Dept Chem, Tianjin 30035, Peoples R China; [Cui, Jin] Tianjin Prod Qual Inspect Technol Res Inst, Natl Foodstuff Inspect Ctr, Tianjin 300384, Peoples R China; [Wang, Yufang] Shijiazhuang Univ Appl Technol, Sci Res Dept, Shijiazhuang 050081, Hebei, Peoples R China in 2021.0, Cited 40.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

A novel metal-organic framework (MOF) with two-dimensional (2D) crystal structure was developed using Cu(NO3)(2)center dot 3H(2)O and 2,2 ‘,5,5 ‘-tetramethoxy-[1,1 ‘-biphenyl]-4,4 ‘-dicarboxylic acid. Further, its structure was characterized using infrared spectroscopy, thermogravimetry, X-ray diffraction, and X-ray crystallography. The activated Cu-MOF was used to catalyze the dehydrogenative oxidation of alcohol and N-arylation of azole compounds. Furthermore, it could be easily recovered and reused.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Application In Synthesis of Benzophenone. In 2021.0 MOLECULES published article about THIOCARBONYL S-METHANIDES; EFFICIENT SYNTHESIS; 1,3-DIPOLAR CYCLOADDITIONS; FERROCENYL THIOKETONES; ALPHA-NITROSOALKENES; HETARYL; ARYL; CHEMISTRY; 1,2-DIAZA-1,3-DIENES; THIOCHALCONES in [Mloston, Grzegorz; Urbaniak, Katarzyna; Sobiecka, Malwina] Univ Lodz, Fac Chem, Dept Organ & Appl Chem, 12 Tamka St, PL-91403 Lodz, Poland; [Heimgartner, Heinz] Univ Zurich, Dept Chem, Winterthurerstr 190, CH-8057 Zurich, Switzerland; [Wuerthwein, Ernst-Ulrich] Westfalische Wilhelms Univ Munster, Organ Chem Inst, Corrensstr 40, D-48149 Munster, Germany; [Wuerthwein, Ernst-Ulrich] Westfalische Wilhelms Univ Munster, Ctr Multiscale Theory & Computat CMTC, Corrensstr 40, D-48149 Munster, Germany; [Zimmer, Reinhold; Lentz, Dieter; Reissig, Hans-Ulrich] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany in 2021.0, Cited 67.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9.

The hetero-Diels-Alder reactions of in situ-generated azoalkenes with thioketones were shown to offer a straightforward method for an efficient and regioselective synthesis of scarcely known N-substituted 1,3,4-thiadiazine derivatives. The scope of the method was fairly broad, allowing the use of a series of aryl-, ferrocenyl-, and alkyl-substituted thioketones. However, in the case of N-tosyl-substituted cycloadducts derived from 1-thioxo-2,2,4,4-tetramethylcyclobutan-3-one and the structurally analogous 1,3-dithione, a more complicated pathway was observed. By elimination of toluene sulfinic acid, the initially formed cycloadducts afforded 2H-1,3,4-thiadiazines as final products. Advanced DFT calculations revealed that the observed high regioselectivity was due to kinetic reaction control and that the (4 + 2)-cycloadditions of sterically less unhindered thiones occurred via highly unsymmetric transition states with shorter C..S-distances (2.27-2.58 angstrom) and longer N..C-distances (3.02-3.57 angstrom). In the extreme case of the sterically very hindered 2,2,4,4-tetramethylcyclobutan-1,3-dione-derived thioketones, a zwitterionic intermediate with a fully formed C-S bond was detected, which underwent ring closure to the 1,3,4-thiadiazine derivative in a second step. For the hypothetical formation of the regioisomeric 1,2,3-thiadiazine derivatives, the DFT calculations proposed more symmetric transition states with considerably higher energies.

Application In Synthesis of Benzophenone. Bye, fridends, I hope you can learn more about C13H10O, If you have any questions, you can browse other blog as well. See you lster.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

An article Nucleophilic Addition and alpha-C-H Substitution Reactions of an Imine Mediated by Dibutylmagnesium and Organolithium Reagents WOS:000669544500006 published article about ORGANOMETALLIC REAGENTS; ASYMMETRIC ALKYLATION; HYDROBORATION; 1,2-ADDITION; COMPLEXES; ALDEHYDES; EFFICIENT; AMINES; BONDS in [Dang, Yan; Wang, Yalan; Li, Yafei; Xu, Man; Jia, Chaohong; Lu, Yanhua; Zhang, Liang; Li, Yahong] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China; [Xia, Yuanzhi] Wenzhou Univ, Coll Chem & Mat Engn, Wenzhou 325035, Peoples R China in 2021.0, Cited 36.0. Quality Control of Benzophenone. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

A series of nucleophilic addition reactions and alpha-C-H substitution reactions of an imine-containing ligand 2-(2-((((1H-pyrrol-2-yl)methylene)amino)methyl)-1H-pyrrol-1-yl) -N,N-d imethylethan-1-amine (HL1) were reported. The reactions of HL1 with 0.5 and 2 equiv of (Bu2Mg)-Bu-n, respectively, gave two complexes of compositions [Mg(L1)(2)] (1) and [Mg-2(L2)(2)] (2) (H2L2 = N-((1-(2- (dimethylamino) ethyl)-1 H-pyrrol-2-yl) methyl)-1-(1H-pyrrol-2-yl)pentan-1-amine). The nucleophilic addition of (Bu2Mg)-Bu-n to the C=N bond of the HL1 ligand occurred in the process for the formation of 2. Treatment of HL1 with 2 and 1 equiv of (BuLi)-Bu-n generated [Li-2(L3)(2)] (3) (HL3 = 2-(2-(((1-(1H-pyrrol-2-yl)-pentylidene)amino)methyl)-1H-pyrrol-1-yl)-N,N-dimethylethan-1-amine) and [Li-2(L1)(2)] (4). An alpha-C-H substitution of the HC=NR moiety of the HL1 ligand triggered by (BuLi)-Bu-n was discovered in the preparation of 3. The formation of 3 demonstrates a new concept for the C-C coupling that involved inert C-H bond activation of HC=NR skeleton. The reactions of HL1 with MeLi, sec-BuLi, and tert-BuLi, respectively, were also examined. The products for both the nucleophilic addition of organolithium reagents to the C=N bond and alpha-C-H substitution of the HC=NR moiety of the HL1 ligand were determined. The mechanisms for the formations of 2 and 3 were rationalized by DFT calculations. The hydroboration reactions catalyzed by 2 were investigated, and these reactions characterize ample substrate scope, very good yields, and high selectivity.

Quality Control of Benzophenone. Bye, fridends, I hope you can learn more about C13H10O, If you have any questions, you can browse other blog as well. See you lster.

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

Product Details of 119-61-9. Authors Zhang, H; Xu, T; Li, DD; Cheng, T; Chen, J; Zhou, Y in ELSEVIER published article about in [Zhang, Hua] Xian Univ Technol, Sch Mat Sci & Engn, Xian 710048, Peoples R China; [Zhang, Hua; Xu, Ting; Chen, Jing; Zhou, Yang] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Cixi Inst Biomed Engn, Ningbo 315201, Peoples R China; [Li, Dongdong] Nanjing Forestry Univ, Coll Chem Engn, 159 Long Pan Rd, Nanjing 210037, Peoples R China; [Cheng, Tao] Pharmaron Ningbo Technol Dev Co Ltd, Ningbo 315366, Peoples R China in 2021.0, Cited 37.0. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

A novel series of bis Indy-NHC gold complexes have been developed and investigated via a mild Agcarbene transfer route. The obtained complexes were characterized by NMR spectroscopy and X-ray diffraction analysis. The catalytic property of these gold complexes was further evaluated in the oxidation of benzylic. The gold complex E1 showed a high catalytic activity in the oxidation of various benzylic substrates, resulting in the corresponding carbonyl compounds with excellent yields using TBHP as oxidant. (C) 2021 Elsevier B.V. All rights reserved.

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

I found the field of Life Sciences & Biomedicine – Other Topics; Computer Science very interesting. Saw the article Phytotoxic property of metabolites isolated from Garcinia gardneriana published in 2021.0. Application In Synthesis of Benzophenone, Reprint Addresses dos Santos, MH (corresponding author), Univ Fed Vicosa, Dept Quim, Ave Peter Henry Rolfs S-N,Campus Univ, BR-36570900 Vicosa, MG, Brazil.. The CAS is 119-61-9. Through research, I have a further understanding and discovery of Benzophenone

Garcinia gardneriana is a medicinal tree species used in Brazil in the treatment of hepatitis and gastritis. This use is attributed to phenolic compounds, mainly 7-epiclusianone, guttiferone-A and fukugetin, which present several proven biological activities. However, to the best of our knowledge, no study on the phytotoxic activity of G. gardneriana extracts has been conducted until now. This research proposed to isolate and quantify by highperformance liquid chromatography (HPLC) the major compounds from G. gardneriana seed extracts in ethyl acetate and to evaluate their phytotoxic activities. The natural products 7-epiclusianone, guttiferone-A and fukugetin were quantified at concentrations varying from 0.46 to 1.13 mg mL-1 and were isolated with yields ranging from 7% to 23% (w/w). The phytotoxic assay indicated that the crude extract showed no action on the dry matter of Sorghum bicolor plants, but the isolated compounds fukugetin and 7-epiclusianone had moderate activity. On the other hand, guttiferone-A displayed a greater herbicide activity than glyphosate, a positive control, even in almost three times lower concentrations, causing severe intoxication in the plants. This work is the first report on this activity by the extract of G. gardneriana and its isolated compounds. Besides that, guttiferone-A showed up as a scaffold for the development of new agrochemicals. Complementing these findings, computational studies suggested that this benzophenone can interact effectively with transferase enzymes type, in special caffeic acid O-methyltransferase from S. bicolor (PDB code: 4PGH), indicating a possible mechanism of action in this plant.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Category: thiomorpholine. Authors Hu, YY; Shao, Y; Zhang, SW; Yuan, Y; Sun, Z; Yuan, Y; Jia, XD in PERGAMON-ELSEVIER SCIENCE LTD published article about in [Hu, Yingying; Zhang, Shuwei; Yuan, Yuan; Sun, Zheng; Yuan, Yu; Jia, Xiaodong] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China; [Shao, Yu] Yangzhou Univ, Sch Informat Engn, Huayang West Rd 196, Yangzhou 225127, Jiangsu, Peoples R China in 2021, Cited 43. The Name is Benzophenone. Through research, I have a further understanding and discovery of 119-61-9

A sp(3) C-H bond functionalization and C – C bond cleavage were realized by AIBN/0 2 catalyst system, providing a series of benzophenones under mild reaction conditions. The mechanistic study shows that a peroxide intermediate is involved in this transformation, and in the case of diphenylmethanes, the sp(3) C-C bond is cleaved through the peroxide rearrangement, which might provides a new way to cleave relatively strong C-C bond and be applied to more general C-C bond activation. (C) 2021 Elsevier Ltd. All rights reserved.

Category: thiomorpholine. Bye, fridends, I hope you can learn more about C13H10O, If you have any questions, you can browse other blog as well. See you lster.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

I found the field of Chemistry very interesting. Saw the article Development of an efficient, one-pot, multicomponent protocol for synthesis of 8-hydroxy-4-phenyl-1,2-dihydroquinoline derivatives published in 2021. COA of Formula: C7H5NO3, Reprint Addresses Tabassum, R; Ashfaq, M (corresponding author), Islamia Univ Bahawalpur, Dept Chem, Bahawalpur 36100, Pakistan.. The CAS is 99-61-6. Through research, I have a further understanding and discovery of 3-Nitrobenzaldehyde

A one-pot quick and efficient multicomponent reaction has been developed for the synthesis of a new series of functionalized 8-hydroxy-4-phenyl-1,2-dihydroquinoline derivatives using 30 mol% ammonium acetate in ethanol as solvent. This economical protocol run smoothly to give variety of quinoline derivatives in 55% to 98% yield from inexpensive reagents and catalyst in mild reaction conditions. Various spectroscopic techniques like FTIR, H-1 NMR and C-13 NMR, MALDI-TOF-MS, and EI-MS were used to study and confirm their structure.

COA of Formula: C7H5NO3. Bye, fridends, I hope you can learn more about C7H5NO3, If you have any questions, you can browse other blog as well. See you lster.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Ticconi, B; Capocasa, G; Cerrato, A; Di Stefano, S; Lapi, A; Marincioni, B; Olivo, G; Lanzalunga, O in ROYAL SOC CHEMISTRY published article about HYDROGEN-PEROXIDE; C-H; POLYAZADENTATE COMPLEXES; SELECTIVE HYDROXYLATION; IRON(IV)-OXO COMPLEXES; EFFICIENT CATALYSTS; BENZOIC-ACIDS; OXIDATION; BENZENE; PHENOL in [Ticconi, Barbara; Capocasa, Giorgio; Cerrato, Andrea; Di Stefano, Stefano; Lapi, Andrea; Marincioni, Beatrice; Lanzalunga, Osvaldo] Univ Roma La Sapienza, Dipartimento Chim, Ple A Moro 5, I-00185 Rome, Italy; [Ticconi, Barbara; Capocasa, Giorgio; Cerrato, Andrea; Di Stefano, Stefano; Lapi, Andrea; Marincioni, Beatrice; Lanzalunga, Osvaldo] Univ Roma La Sapienza, Dipartimento Chim, Sez Meccanismi Reaz, Ist CNR & Sistemi Biol ISB CNR, Ple A Moro 5, I-00185 Rome, Italy; [Olivo, Giorgio] Univ Girona, Inst Quim Computac & Catalisi IQCC, Campus Montilivi,C Maria Aurelia Capmany 69, Girona 17003, Spain; [Olivo, Giorgio] Univ Girona, Dept Quim, Campus Montilivi,C Maria Aurelia Capmany 69, Girona 17003, Spain; [Olivo, Giorgio] Univ Girona, Inst Quim Computac & Catalisi IQCC, Campus Montilivi, Girona 17071, Spain; [Olivo, Giorgio] Univ Girona, Dept Quim, Campus Montilivi, Girona 17071, Spain in 2021, Cited 75. Product Details of 90-44-8. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

The oxidation of a series of alkylaromatic compounds with H2O2 catalyzed by an imine-based non-heme iron complex prepared in situ by reaction of 2-picolylaldehyde, 2-picolylamine, and Fe(OTf)(2) in a 2 : 2 : 1 ratio leads to a marked chemoselectivity for aromatic ring hydroxylation over side-chain oxidation. This selectivity is herein investigated in detail. Side-chain/ring oxygenated product ratio was found to increase upon decreasing the bond dissociation energy (BDE) of the benzylic C-H bond in line with expectation. Evidence for competitive reactions leading either to aromatic hydroxylation via electrophilic aromatic substitution or side-chain oxidation via benzylic hydrogen atom abstraction, promoted by a metal-based oxidant, has been provided by kinetic isotope effect analysis.

Product Details of 90-44-8. Welcome to talk about 90-44-8, If you have any questions, you can contact Ticconi, B; Capocasa, G; Cerrato, A; Di Stefano, S; Lapi, A; Marincioni, B; Olivo, G; Lanzalunga, O or send Email.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

Authors Kharrngi, B; Dhar, ED; Basumatary, G; Das, D; Deka, RC; Yadav, AK; Bez, G in INDIAN ACAD SCIENCES published article about in [Kharrngi, Balamphrang; Basumatary, Grace; Bez, Ghanashyam] NE Hill Univ, Dept Chem, Shillong 793022, Meghalaya, India; [Dhar, Errini Decruse; Yadav, Arun K.] NE Hill Univ, Dept Zool, Shillong 793022, Meghalaya, India; [Das, Dharitri; Deka, Ramesh Ch] Tezpur Univ, Dept Chem Sci, Tezpur 784028, Assam, India in 2021, Cited 66. Quality Control of 3-Nitrobenzaldehyde. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6

Due to serious side effects of benzimidazoles such as apoptosis and mitotic arrest, development of alternative anthelmintic drugs with comparable efficacy to target the acetylcholine receptors of parasites is considered very important to control this parasitic disease. Here we have developed an excellent method for synthesis of biscoumarins by employing a mild and efficient proline derived bifunctional thiourea catalyst bearing pyrrolidine and thiourea catalytic sites and tested their anthelmintic activity against helminth parasites Raillietina echinobothrida and Syphacia obvelata. The compounds 2a, 2j, 2k and 2o demonstrated much stronger anthelmintic activity against Raillietina echinobothrida in comparison to the standard drug, Praziquantel. Molecular docking simulations of the optimized compounds with beta -tubulin showed excellent binding interactions with several amino acid residues of the active site and the docking scores with beta -tubulin were found to be comparable to the in vitro anthelmintic activity.Graphical AbstractA series of biscoumarins were synthesized and they showed excellent anthelmintic properties in comparison to conventional benzimidazoles.

Welcome to talk about 99-61-6, If you have any questions, you can contact Kharrngi, B; Dhar, ED; Basumatary, G; Das, D; Deka, RC; Yadav, AK; Bez, G or send Email.. Quality Control of 3-Nitrobenzaldehyde

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