Category: 100-19-6

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

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 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

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.

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

Product Details of 100-19-6. In 2019.0 ORG LETT published article about 2-AMINOINDOLIZINES; CYCLOADDITION in [Rossler, Matthew D.; Hartgerink, Colin T.; Zerull, Emily E.; Boss, Benjamin L.; Frndak, Abigail K.; Mason, Miles M.; Nickerson, Leslie A.; Romero, Evan O.; Van de Burg, Jaimie E.; Staples, Richard J.; Anderson, Carolyn E.] Calvin Coll, Dept Chem & Biochem, Grand Rapids, MI 49546 USA; [Nickerson, Leslie A.] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA; [Staples, Richard J.] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA in 2019.0, Cited 20.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A new Au(I)-catalyzed method for the preparation of trisubstituted indolizines from easily accessible 2-propargyloxy-pyridines is reported. The reaction tolerates a wide range of functionality, allowing for diversity to be introduced in four distinct regions of the product (R, R-1, R-2, and Ar). The proposed mechanism proceeds via enol addition to an allenamide intermediate and explains the observed increase in yields when electron poor methyl ketones are utilized.

Product Details of 100-19-6. 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

SDS of cas: 100-19-6. Huynh, TV; Doan, KV; Luong, NTK; Nguyen, DTP; Doan, SH; Nguyen, TT; Phan, NTS in [Huynh, Tien, V; Doan, Khang, V; Luong, Ngoc T. K.; Nguyen, Duyen T. P.; Doan, Son H.; Nguyen, Tung T.; Phan, Nam T. S.] Ho Chi Minh City Univ Technol HCMUT, Fac Chem Engn, 268 Ly Thuong Kiet,Dist 10, Ho Chi Minh City, Vietnam; [Huynh, Tien, V; Doan, Khang, V; Luong, Ngoc T. K.; Nguyen, Duyen T. P.; Doan, Son H.; Nguyen, Tung T.; Phan, Nam T. S.] Vietnam Natl Univ Ho Chi Minh City, Linh Trung Ward, Ho Chi Minh City, Vietnam; [Huynh, Tien, V; Luong, Ngoc T. K.; Nguyen, Duyen T. P.] Ho Chi Minh City Univ Food Ind HUFI, Fac Chem Technol, 140 Le Trang Tan, Ho Chi Minh City, Vietnam published New synthesis of 2-aroylbenzothiazoles via metal-free domino transformations of anilines, acetophenones, and elemental sulfur in 2020.0, Cited 43.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

A new synthesis of 2-aroylbenzothiazoles via iodine-promoted domino transformations of anilines, acetophenones, and elemental sulfur was demonstrated. The highlights of this tandem synthesis are (1) easily available anilines and acetophenones as feedstock; (2) transition metal-free conditions; (3) inexpensive, nontoxic, easy handling, and abundant elemental sulfur as a building block. This synthetic strategy would complement the existing methods in the synthesis of this important heterocyclic scaffold. To our best knowledge, the formation of 2-aroylbenzothiazoles from simple anilines, acetophenones, and elemental sulfur was not previously reported in the literature.

SDS of cas: 100-19-6. 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

An article Ruthenium-Catalyzed Annulation of N-Cbz Hydrazones via C-H/N-N Bond Activation for the Rapid Synthesis of Isoquinolines WOS:000471236800006 published article about H ACTIVATION; POLYETHYLENE-GLYCOL; ORGANIC-SYNTHESIS; INTERNAL ALKYNES; DIRECTING GROUP; EFFICIENT SYNTHESIS; IRIDIUM COMPLEXES; O BOND; FUNCTIONALIZATION; RHODIUM in [Deshmukh, Dewal S.; Bhanage, Bhalchandra M.] Inst Chem Technol, Dept Chem, N Parekh Marg, Mumbai 400019, Maharashtra, India in 2019.0, Cited 112.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6. Recommanded Product: 1-(4-Nitrophenyl)ethanone

In this work, N-Cbz hydrazone has been employed as a rarely explored directing group for the synthesis of isoquinolines by annulation with internal alkynes via C-H/ N-N activation using Ru catalyst. Additive as well as external oxidant-free rapid protocol has been established for the synthesis of isoquinolines using microwave strategy. Use of non-volatile and biodegradable PEG as a green solvent with lower catalyst loading makes the proposed protocol environmentally benign. Further, higher functional group tolerance and wide substrate scope has been observed under the stated methodology with higher yields.

Recommanded Product: 1-(4-Nitrophenyl)ethanone. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Deshmukh, DS; Bhanage, BM or concate me.

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

Name: 1-(4-Nitrophenyl)ethanone. In 2019.0 ORG BIOMOL CHEM published article about DOUBLE CARBONYLATION; TERMINAL ALKYNES; C-H; ENANTIOSELECTIVE SYNTHESIS; OXIDATIVE AMIDATION; OXOCARBOXYLIC ACIDS; CHLOROPEPTIN-I; FKBP12 LIGANDS; ARYL IODIDES; DERIVATIVES in [Li, Ping-Gui; Zhu, Hao; Fan, Min; Yan, Cheng; Shi, Kai; Chi, Xi-Wen; Zou, Liang-Hua] Jiangnan Univ, Minist Educ, Sch Pharmaceut Sci, Key Lab Carbohydrate Chem & Biotechnol, Lihu Ave 1800, Wuxi 214122, Jiangsu, Peoples R China; [Li, Ping-Gui] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Xianlin Ave 163, Nanjing 210093, Jiangsu, Peoples R China in 2019.0, Cited 76.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

Copper-catalyzed coupling of alpha-keto acids with anthranils is reported for the synthesis of alpha-ketoamides. This process involves N-O/C-O bond cleavages and C-N bond formation. Furthermore, the decarboxylation of alpha-keto acids can be successfully suppressed under redox-neutral conditions.

Welcome to talk about 100-19-6, If you have any questions, you can contact Li, PG; Zhu, H; Fan, M; Yan, C; Shi, K; Chi, XW; Zou, LH or send Email.. Name: 1-(4-Nitrophenyl)ethanone

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

Authors Nguyen, DP; Sladek, RN; Do, LH in PERGAMON-ELSEVIER SCIENCE LTD published article about TRANSFER HYDROGENATION; CARBONYL-COMPOUNDS; LEVULINIC ACID; PRIMARY AMINES; KETONES; ALDEHYDES; ALKYLATION; AMMONIA; HALIDES in [Nguyen, Dat P.; Sladek, Rudolph N.; Do, Loi H.] Univ Houston, Dept Chem, Univ Pk, Houston, TX 77004 USA in 2020.0, Cited 44.0. 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 conversion of aldehydes and ketones to 1 degrees amines could be promoted by half-sandwich iridium complexes using ammonium formate as both the nitrogen and hydride source. To optimize this method for green chemical synthesis, we tested various carbonyl substrates in common polar solvents at physiological temperature (37 degrees C) and ambient pressure. We found that in methanol, excellent selectivity for the amine over alcohol/amide products could be achieved for a broad assortment of carbonyl-containing compounds. In aqueous media, selective reduction of carbonyls to 1 degrees amines was achieved in the absence of acids. Unfortunately, at Ir catalyst concentrations of <1 mM in water, reductive amination efficiency dropped significantly, which suggest that this catalytic methodology might be not suitable for aqueous applications where very low catalyst concentration is required (e.g., inside living cells). (C) 2020 Elsevier Ltd. All rights reserved. Product Details of 100-19-6. About 1-(4-Nitrophenyl)ethanone, If you have any questions, you can contact Nguyen, DP; Sladek, RN; Do, LH or concate me.

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

Category: benzodioxans. Safari, J; Shokrani, Z; Zarnegar, Z in [Safari, Javad; Shokrani, Zahra] Univ Kashan, Coll Chem & Biochem, Dept Organ Chem, Lab Organ Compound Res, Kashan, IR, Iran; [Zarnegar, Zohre] Univ Payame Noor, Dept Chem, Res Affiliate, Tehran, Iran published Asparagine as a Green Organocatalyst for the Synthesis of 2-Aminothiazoles in 2020.0, Cited 23.0. The Name is 1-(4-Nitrophenyl)ethanone. Through research, I have a further understanding and discovery of 100-19-6.

In this research, an efficient method for the one-pot synthesis of 2-aminothiazolesviathe reaction of thiourea with methylcarbonyls in the presence of iodine as an oxidant reagent has been developed using asparagine as a green organocatalyst at 80 degrees C in DMSO solvent. Advantages of this efficient method include greener and cleaner conditions, easy isolation of products, higher purity and excellent yield of products, and convenient manipulation.

Welcome to talk about 100-19-6, If you have any questions, you can contact Safari, J; Shokrani, Z; Zarnegar, Z or send Email.. Category: benzodioxans

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