Heterocyclic Building Blocks-benzodioxan

Product Details of 100-19-6. In 2019.0 J HETEROCYCLIC CHEM published article about BEARING BENZOTHIAZOLE; ANTITUMOR-ACTIVITY; IN-VITRO; DERIVATIVES; THIOPHENE; PYRIDINE; HETEROCYCLES; INHIBITORS; THIAZOLE; MOIETY in [Hassan, Aisha Y.] Al Azhar Univ, Fac Sci Girls, Dept Chem, Cairo, Egypt; [Sarg, Marwa T.; Hussein, Ebtehal M.] Al Azhar Univ, Fac Sci Girls, Dept Pharmaceut Organ Chem, Cairo, Egypt in 2019.0, Cited 45.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

On the pharmaceutical account of the reported anticancer activity of benzothiazole derivatives, differently substituted benzothiazole derivatives 2a-c to 34a,b, attached at 2-position to different heterocyclic moieties, were synthesized via different chemical reactions. Thirteen of the newly synthesized compounds were selected by the National Cancer Institute, Bethesda, Maryland, USA, and evaluated for their in vitro antitumor activity against 60 human tumor cell lines in a one-dose screening panel among which two compounds 4 and 17 showed high activity and were selected for further evaluation in the five-dose full panel assay, in which compound 4 exerted powerful growth inhibitory activity against all cell lines with GI(50) ranging from 0.683 to 4.66 mu M/L in addition to excellent lethal activity against most of the cell lines.

Product Details of 100-19-6. Welcome to talk about 100-19-6, If you have any questions, you can contact Hassan, AY; Sarg, MT; Hussein, EM or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Copper-Catalyzed Site-Selective Oxidative C-C Bond Cleavage of Simple Ketones for the Synthesis of Anilides and Paracetamol WOS:000455542500016 published article about METHYL KETONES; CARBONYLATION REACTIONS; CARBOXYLIC-ACIDS; N-ACYLATION; AMIDES; AMINES; ALCOHOLS; REARRANGEMENT; AMIDATION; CARBON in [Vodnala, Nagaraju; Gujjarappa, Raghuram; Kaldhi, Dhananjaya; Kabi, Arup. K.; Malakar, Chandi C.] Natl Inst Technol Manipur, Dept Chem, Imphal 795004, Manipur, India; [Hazra, Chinmoy K.] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 305701, South Korea; [Beifuss, Uwe] Univ Hohenheim, Inst Chem, Garbenstr 30, D-70599 Stuttgart, Germany in 2019, Cited 70. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Computed Properties of C8H7NO3

A copper-catalyzed approach for the N-acylation of anilines with acetone and acetophenones via C-C bond cleavage is described. Under the developed conditions both CHCl3 and CH2Cl2 were identified as potential C1-source to promote the transformation. The reaction features a site selective C-C bond cleavage to install the amide moieties with high functional-group compatibility and wide substrate scope. The developed method avoids the use of sensitive and narcotic agents. The method also represents an excellent complement to the previous protocols with lower E-factor (13.91 mg/1 mg) than current industrially used method (E-factor 17.54 mg/1 mg). The developed approach has also been extended for the effective preparation of pyridine derivatives and paracetamol in gram scale. The course of the reaction was monitored by H-1 NMR as a preliminary investigation of the reaction mechanism.

Computed Properties of C8H7NO3. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Vodnala, N; Gujjarappa, R; Hazra, CK; Kaldhi, D; Kabi, AK; Beifuss, U; Malakar, CC or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

In 2019.0 J ORG CHEM published article about C-H ALKYLATION; ENANTIOSELECTIVE SYNTHESIS; SECONDARY AMIDES; DERIVATIVES; 4-PYRIDONE; 2-PYRIDONES; INHIBITORS; SULFOXIDES; OLIGOMERS; ANHYDRIDE in [Huang, Jingjia; Hu, Gang; An, Shaoyu; Chen, Dongding; Li, Minglei; Li, Pingfan] Beijing Univ Chem Technol, Fac Sci, Dept Organ Chem, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China; [Hu, Gang] Baotou Teachers Coll, Dept Chem, Baotou 014030, Peoples R China in 2019.0, Cited 72.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Product Details of 100-19-6

N-Alkylated 4-pyridones were obtained through a one-pot procedure involving either normal or interrupted Pummerer reactions between triflic anhydride-activated sulfoxides and 4-fluoropyridine derivatives, followed by hydrolysis. On the other hand, triflic anhydride-activated benzyl 6-fluoro-2-pyridyl sulfoxide could react with alkenes or alkynes to afford thiazolo[3,2-a]pyridin-5-ones, via the pyridinium salt intermediates.

About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Huang, JJ; Hu, G; An, SY; Chen, DD; Li, ML; Li, PF or concate me.. Product Details of 100-19-6

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Copper-Catalyzed Annulation of Oxime Acetates with alpha-Amino Acid Ester Derivatives: Synthesis of 3-Sulfonamido/Imino 4-Pyrrolin-2-ones WOS:000530076400016 published article about ONE-POT SYNTHESIS; KETOXIME CARBOXYLATES; VINYL AZIDES; CYCLIZATION; DIKETOPYRROLOPYRROLE; STRATEGY; VIOLACEIN; PYRIDINE; FUNCTIONALIZATION; HETEROANNULATION in [Miao, Chun-Bao; Zheng, An-Qi; Zhou, Li-Jin; Lyu, Xinyu; Yang, Hai-Tao] Changzhou Univ, Jiangsu Key Lab Adv Catalyt Mat & Technol, Sch Petrochem Engn, Changzhou 213164, Jiangsu, Peoples R China in 2020.0, Cited 66.0. Recommanded Product: 100-19-6. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A copper-catalyzed annulation of oxime acetates and alpha-amino acid ester derivatives for the easy preparation of 4-pyrrolin-2-ones bearing a 3-amino group has been developed. This process features the oxidation of amines with oxime esters as the internal oxidant to produce the active 1,3-dinucleophilic and 1,2-dielectrophilic species concurrently. The subsequent nucleophilic cyclization realizes the efficient construction of 4-pyrrolin-2-one derivatives.

Welcome to talk about 100-19-6, If you have any questions, you can contact Miao, CB; Zheng, AQ; Zhou, LJ; Lyu, XY; Yang, HT or send Email.. Recommanded Product: 100-19-6

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Synthesis, biological evaluation, and molecular docking studies of novel pyrazole, pyrazoline-clubbed pyridine as potential antimicrobial agents WOS:000604777800001 published article about DERIVATIVES; DESIGN in [Desai, Nisheeth C.; Vaja, Darshita V.; Monapara, Jahnvi D.] Maharaja Krishnakumarsinhji Bhavnagar Univ, Dept Chem DST Fist Sponsored, Div Med Chem, Mahatma Gandhi Campus, Bhavnagar 364002, Gujarat, India; [Manga, Vijjulatha; Vani, Tamalapakula] Osmania Univ, Univ Coll Sci, Dept Chem, Mol Modeling & Med Chem Grp, Hyderabad, India in 2021.0, Cited 24.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Formula: C8H7NO3

We have prepared 15 hybrid pyrazole, pyrazoline-clubbed pyridine-containing compounds (5a-o) and tested for their antibacterial and antifungal activities for the development of potential antimicrobial agents. The structures of this novel series were characterized by various spectral techniques like IR, H-1 NMR, C-13 NMR, LC-MS, and elemental analysis. The synthesized compounds 5d, 5e, 5i, 5k, 5m, and 5o exhibited significant antimicrobial activity in the comparison of standard drugs. Molecular docking studies that have been carried out to emphasize the binding orientations of these molecules were in good compliance with crystal structure interactions. The predicted drug-likeness (ADME) properties were found to be in the acceptable range.

Computed Properties of C8H7NO3. Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Recently I am researching about H BOND OXIDATION; SELECTIVE OXIDATION; ACTIVATION; TOLUENE; OXYGENATION; OZONE, Saw an article supported by the . Published in SCIENCE PRESS in BEIJING ,Authors: Liu, LC; Wu, JQ; Ma, HF; Zhang, H; Gu, JF; Li, YF. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone. Safety of 1-(4-Nitrophenyl)ethanone

A practical method for the oxidation of aromatic side chains was established for the preparation of aromatic aldehydes and ketones. Using NiCl2 as the catalyst, substituted toluenes were oxidized with Na2S2O8 at the benzvlic site for the synthesis of the corresponding aldehydes in the yield of 22%similar to 79%. Ethylbenzene analogs were oxidized more easily to obtain the corresponding ketones with 64%similar to 84% yields. The oxidation of benzyl alcohol analogs was completed to acquire the corresponding carbonyl compounds in shorter time with better selectivity and yields. The method has the advantages such as the mild reaction conditions, no requirement for precious metals or additional promoter, and good selectivity.

Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.. Safety of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Gu, TC; Mo, SY; Mu, YQ; Huang, X; Hu, LM in ELSEVIER SCIENCE SA published article about REACTIVE OXYGEN; SELECTIVE DETECTION; CANCER; EMISSION; ACID in [Gu, Tianchu; Mo, Shanyan; Mu, Yingqi; Huang, Xin; Hu, Liming] Beijing Univ Technol, Coll Life Sci & Bioengn, Beijing Key Lab Environm & Oncol, Beijing 100124, Peoples R China in 2020.0, Cited 54.0. Name: 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

Hydrogen peroxide (H2O2) is a small molecule of reactive oxygen species, mainly produced by cell mitochondria, which plays an important role in physiological processes. Excess of H2O2 in normal cells could causes a variety of diseases. For that reason, it is very significant to emerge a detection method with high-precision for H2O2. Herein, we reported a structurally novel fluorescent probe, para-nitrophenyl oxoacetyl rhodamine (RhB-NIR) for the detection of H2O2 levels in living cells. The results show that the Stokes shift for RhB-NIR is 140 nm, much larger than those for other reported rodamine derivatives. RhB-NIR shows satisfactory specificity and high sensitivity for the detection of H2O2. Excellent linear relationship with H2O2 within a certain concentration range (0-10 mu M) was displayed, and the limit of detection (LOD) is 61 nM. More importantly, RhB-NIR realized fluorescence imaging of H2O2 in living cells. In addition, RhB-NIR also shows great potential for targeting mitochondria in cell colocalization experiments, in which the Pearson’s coefficient is 0.91 using Rhodamine 123 as a reference. This probe will be a promising tool for detecting H2O2 in the future research.

Welcome to talk about 100-19-6, If you have any questions, you can contact Gu, TC; Mo, SY; Mu, YQ; Huang, X; Hu, LM or send Email.. Name: 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Recommanded Product: 1-(4-Nitrophenyl)ethanone. In 2020.0 EUR J ORG CHEM published article about C-H-FUNCTIONALIZATION; DEHYDROGENATIVE COUPLING APPROACH; METAL-FREE; OLEFIN SYNTHESIS; BOND ACTIVATION; METHYL KETONES; OXIDATIVE AMINATION; MICHAEL ADDITION; IODINE; AMINES in [Rastogi, Gaurav K.; Deka, Bhaskar; Deb, Mohit L.; Baruah, Pranjal K.] Gauhati Univ, GUIST, Dept Appl Sci, Gauhati 781014, Assam, India; [Rastogi, Gaurav K.] NEIST, CSIR, Dept Appl Organ Chem, Jorhat 785006, Assam, India in 2020.0, Cited 91.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

We have developed an efficient metal-free route for the synthesis of 1,4-enedione derivatives under microwave irradiation by reacting easily available arylmethylketones with DMSO or diphenyl sulfoxide in the presence of TBAI and persulfate. The reaction is very clean and completes within very short time. All the reagents and catalysts are cheap and environmentally benign. In addition, the E-isomer of the products can easily be transformed into the Z-isomer by using eosin Y photocatalyst under the irradiation of white CFL.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. Welcome to talk about 100-19-6, If you have any questions, you can contact Rastogi, GK; Deka, B; Deb, ML; Baruah, PK or send Email.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

Authors Yang, SX; Yao, L; Fan, ZH; Han, J; Chen, J; He, WM; Deng, HM; Shao, M; Zhang, H; Cao, WG in ELSEVIER SCIENCE SA published article about EXO SELECTIVITY; ALDER; CONSTRUCTION; HETEROCYCLES; INHIBITORS in [Yang, Shanxue; Fan, Zhenhua; Han, Jing; Chen, Jie; He, Weimin; Zhang, Hui; Cao, Weiguo] Shanghai Univ, Innovat Drug Res Ctr, Dept Chem, Shanghai 200444, Peoples R China; [Yao, Lan] Shanghai Blood Ctr, Inspect Dept, Shanghai 200051, Peoples R China; [Deng, Hongmei; Shao, Min; Zhang, Hui] Shanghai Univ, Lab Microstruct, Instrumental Anal & Res Ctr, Shanghai 200444, Peoples R China; [Cao, Weiguo] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China in 2021.0, Cited 39.0. Product Details of 100-19-6. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

The highly diastereoselective synthesis of perfluoroalkyl-containing pyrano[3,4-c]pyrroles has been accomplished via a cascade process involving Michael addition, Passerini-type reaction, Mumm rearrangement and an oxo-Diels-Alder reaction. This domino transformation of isocyanides, methyl perfluoroalk-2-ynoates and 3-aroyl (or heteroyl) acrylic acids proceeded smoothly at room temperature and led to the formation of the highly diastereoselective target compounds with high functional-group compatibility in good to excellent yields.

Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Yang, SX; Yao, L; Fan, ZH; Han, J; Chen, J; He, WM; Deng, HM; Shao, M; Zhang, H; Cao, WG or concate me.

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem

An article Magnetic Fe-Cr-Ni oxide alloy nano-belts prepared from the chemical decomposition of a stainless steel screw (a top-down approach): an efficient and cheap catalyst for multicomponent reactions WOS:000519963900003 published article about ONE-POT SYNTHESIS; FRIEDLANDER SYNTHESIS; NANOPARTICLES; COMPLEX; SURFACE; ACID; NANOCATALYST; DERIVATIVES; QUINOLINES; PHOSPHINE in [Kazemnejadi, Milad; Zeinali, Atefeh; Nasseri, Mohammad Ali] Univ Birjand, Dept Chem, Fac Sci, Birjand 97175615, Iran; [Sharafi, Zeinab] Lorestan Univ Med Sci, Razi Herbal Med Res Ctr, Khorramabad, Iran; [Mahmoudi, Boshra] Sulaimani Polytech Univ, Res Ctr, Sulaimani 46001, Kurdistan Regio, Iraq in 2020.0, Cited 48.0. Quality Control of 1-(4-Nitrophenyl)ethanone. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6

A new, cheap, and accessible method has been used for the preparation of nano-belts from the chemical decomposition (top-down approach) of a cheap stainless steel screw and found as an efficient magnetically recyclable nanocatalyst for the preparation of quinolines and 1,8-dioxo-octahydroxanthenes under mild reaction conditions. The nano-belts, Fe-Cr-Ni oxide alloy, was prepared in a two-step synthesis and characterized with various instrumental methods. Due to magnetic property of the screw (a ferritic-alloy), the resultant nano-belts is magnetic. Magnetic Fe-Cr-Ni alloy nano-belts were applied toward efficient preparation of quinolines and 1,8-dioxo-octahydroxanthenes under mild conditions. The catalyst could be readily recovered and recycled for several consecutive runs, while it suffers from a very low metal leaching and subsequently efficiency drop. Graphic abstract

Bye, fridends, I hope you can learn more about C8H7NO3, If you have any questions, you can browse other blog as well. See you lster.. Quality Control of 1-(4-Nitrophenyl)ethanone

Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem