What about chemistry interests you the most Phenyl(pyridin-2-yl)methanone

Welcome to talk about 91-02-1, If you have any questions, you can contact Hou, CF; Sun, SE; Liu, ZQ; Zhang, H; Liu, Y; An, Q; Zhao, J; Ma, JJ; Sun, ZZ; Chu, WY or send Email.. SDS of cas: 91-02-1

SDS of cas: 91-02-1. Authors Hou, CF; Sun, SE; Liu, ZQ; Zhang, H; Liu, Y; An, Q; Zhao, J; Ma, JJ; Sun, ZZ; Chu, WY in WILEY-V C H VERLAG GMBH published article about in [Hou, Chuanfu; Sun, Shouneng; Liu, Ziqi; Zhang, Hui; Liu, Yue; An, Qi; Zhao, Jian; Ma, Junjie; Sun, Zhizhong; Chu, Wenyi] Heilongjiang Univ, Sch Chem & Mat Sci, Harbin 150080, Peoples R China in 2021.0, Cited 80.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1

Herein, the development of a visible-light-induced catalytic system to achieve the decarboxylative acylation of pyridine N-oxides with alpha-oxocarboxylic acids, at room temperature and using the organic dye fluorescein dimethylammonium as a new type of photocatalyst, is reported. A series of 2-arylacylpyridine N-oxides were selectively synthesized in moderate to good yields by controlling the polarity of the reaction solvent. The developed strategy was successfully applied in the synthesis of an important intermediate of the drug, acrivastine, on a gram scale. Notably, this is the first time that fluorescein dimethylammonium has been used to catalyze the Minisci-type C-H decarboxylative acylation reaction. The mechanism of decarboxylative acylation was studied by capturing adducts of acyl radicals and 1,1-diphenylethylene to confirm a radical mechanism. The disclosed catalytic system provides a green synthetic strategy for decarboxylative acylation without the use of additional oxidants or metal catalysts.

Welcome to talk about 91-02-1, If you have any questions, you can contact Hou, CF; Sun, SE; Liu, ZQ; Zhang, H; Liu, Y; An, Q; Zhao, J; Ma, JJ; Sun, ZZ; Chu, WY or send Email.. SDS of cas: 91-02-1

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

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Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.. Formula: C12H9NO

Bocian, A; Gorczynski, A; Marcinkowski, D; Witomska, S; Kubicki, M; Mech, P; Bogunia, M; Brzeski, J; Makowski, M; Pawluc, P; Patroniak, V in [Bocian, Aleksandra; Gorczynski, Adam; Witomska, Samanta; Kubicki, Maciej; Pawluc, Piotr; Patroniak, Violetta] Adam Mickiewicz Univ, Fac Chem, Uniwersytetu Poznanskiego 8, PL-61614 Poznan, Poland; [Marcinkowski, Damian; Pawluc, Piotr] Wroclaw Univ Econ, Komandorska 118-120, PL-53345 Wroclaw, Poland; [Witomska, Samanta] Wielkopolska Ctr Adv Technol, Uniwersytetu Poznanskiego 10, PL-61614 Poznan, Poland; [Mech, Paulina; Bogunia, Malgorzata; Brzeski, Jakub; Makowski, Mariusz] Univ Gdansk, Fac Chem, Dept Bioinorgan Chem, W Stwosza 63, PL-80308 Gdansk, Poland published New benzothiazole based copper(II) hydrazone Schiff base complexes for selective and environmentally friendly oxidation of benzylic alcohols: The importance of the bimetallic species tuned by the choice of the counterion in 2020.0, Cited 63.0. Formula: C12H9NO. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

Green and sustainable chemistry approaches necessitate an ongoing investigation towards new, environmentally benign and selective catalysts. We have thus prepared a new benzothiazole-scaffolded hydrazone Schiff base ligand L and coordinated it with copper(II) ions leading to five different complexes, the form of which in the solid state is counterion-dependent. Nitrate, chloride and trifiate anions lead to monometallic species, whereas utilization of sulfates and tetrafluoroborates is responsible for the formation of bimetallic assemblies. The catalytic efficiency of synthesized compounds was shown in Cu-TEMPO (2,2,6,6-tetramethyl-l-piperidinoxyl) aerobic oxidation of activated alcohols resulting in good to excellent conversions and 100% selectivity to form the corresponding aldehydes. Considering the experimental results and Density Functional Theory calculations we propose two most plausible reaction mechanisms that further corroborate the enhanced activity of bimetallic species. It appears that the tridentate character of the ligand sacrifices some of the overall catalytic efficiency for the selectivity of the process. Aqueous reaction medium, low catalyst loading, air as oxidant and exclusive oxidative selectivity render these Cu ll complexes promising candidates for further improvement. (C) 2020 Elsevier B.V. All rights reserved.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

An update on the compound challenge: C12H9NO

Welcome to talk about 91-02-1, If you have any questions, you can contact Jiang, G; Lin, Y; Cai, MZ; Zhao, H or send Email.. Product Details of 91-02-1

I found the field of Chemistry very interesting. Saw the article Recyclable Heterogeneous Copper(II)-Catalyzed Oxidative Cyclization of 2-Pyridine Ketone Hydrazones Towards [1,2,3]Triazolo[1,5-a]pyridines published in 2019.0. Product Details of 91-02-1, Reprint Addresses Zhao, H (corresponding author), Guangdong Pharmaceut Univ, Guangdong Cosmet Engn & Technol Res Ctr, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China.; Cai, MZ (corresponding author), Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China.. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

The heterogeneous copper(II)-catalyzed oxidative cyclization of 2-pyridine ketone hydrazones was achieved in ethyl acetate at room temperature in the presence of an MCM-41-anchored bidentate 2-aminoethylamino copper(II) catalyst [MCM-41-2N-Cu(OAc) (2) ], in the presence of air as the oxidant, yielding a wide variety of [1,2,3]triazolo[1,5- a ]pyridines in mostly good to high yields. The present method was also applied to the direct one-pot synthesis of [1,2,3]triazolo[1,5- a ]pyridines from 2-acylpyridine derivatives and hydrazine monohydrate. Importantly, this supported copper(II) catalyst could be conveniently obtained via a simple procedure from easily available and inexpensive reagents, recovered by filtration of the reaction mixture, and reused at least seven times without a significant loss of catalytic activity.

Welcome to talk about 91-02-1, If you have any questions, you can contact Jiang, G; Lin, Y; Cai, MZ; Zhao, H or send Email.. Product Details of 91-02-1

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

What advice would you give a new faculty member or graduate student interested in a career Phenyl(pyridin-2-yl)methanone

Recommanded Product: 91-02-1. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.

Yang, J; Deng, YF; Zhang, YZ in [Yang, Jiong; Deng, Yi-Fei; Zhang, Yuan-Zhu] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China published Two azido-bridged homospin Fe(ii)/Co(ii) coordination polymers featuring single-chain magnet behavior in 2020.0, Cited 72.0. Recommanded Product: 91-02-1. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

Two azido-bridged homospin Fe(ii)/Co(ii) coordination polymers [Fe-2(Bzp)(2)(N-3)(4)](n) (1) and [Co-4(Bzp)(4)(N-3)(8)(MeOH)(2)](n) (2) (bzp = 2-benzoylpyridine) are prepared, which consist of one-dimensional neutral chains with pure EO-azido (mu(2)-1,1-N-3) bridges. Magnetically, both 1 and 2 exhibit considerable intrachain ferromagnetic interactions which benefit from the EO-azido bridging mode, leading to typical single-chain magnet (SCM) behavior under both the infinite-size and finite-size regime and pronounced hysteresis loops. As far as the bridging network is concerned, complex 1 represents not only a rare example of homospin Fe(ii)-based SCMs but also the first Fe(ii) chain compound with pure EO-azido bridges.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

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Computed Properties of C12H9NO. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.

Computed Properties of C12H9NO. In 2020.0 ORG LETT published article about SELECTIVE REDUCTION; LABELED COMPOUNDS; HYDROGEN ISOTOPE; PRIMARY ALCOHOLS; DEUTERIUM; ACTIVATION; TRITIATION; DISCOVERY; SYSTEM; MILD in [Zhu, Nengbo; Su, Min; Wan, Wen-Ming; Li, Yajun; Bao, Hongli] Chinese Acad Sci, Ctr Excellence Mol Synth, Fujian Inst Res Struct Matter, State Key Lab Struct Chem,Key Lab Coal Ethylene G, Fuzhou 350002, Peoples R China in 2020.0, Cited 59.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

alpha-Deuterated alcohols have important applications in pharmaceuticals and mechanism studies. Here, we report a new and practical strategy for the reductive deuteration of ketones using a Mg/BrCH2CH2Br/D2O system, which affords alpha-deuterated alcohols in good yields and with almost quantitative incorporation of deuterium. The synthetic value of this method has been demonstrated by the easy access to deuterated drugs or drug derivatives. This method may inspire the discovery of other deuterium-containing drugs.

Computed Properties of C12H9NO. Bye, fridends, I hope you can learn more about C12H9NO, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

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Safety of Phenyl(pyridin-2-yl)methanone. Welcome to talk about 91-02-1, If you have any questions, you can contact Dohmen, C; Ihmels, H; Kreienmeier, R; Patrick, BO or send Email.

Safety of Phenyl(pyridin-2-yl)methanone. In 2019.0 CHEM COMMUN published article about CONFORMATIONAL POLYMORPHISM; PHOTOPHYSICAL PROPERTIES; EFFICIENT SYNTHESIS; OPTICAL-PROPERTIES; CASCADE APPROACH; COLOR; CHROMOPHORES; HETEROCYCLES in [Dohmen, Christoph; Ihmels, Heiko; Kreienmeier, Rouven] Univ Siegen, Dept Chem Biol Organ Chem 2, Adolf Reichwein Str 2, D-57068 Siegen, Germany; [Patrick, Brian O.] Univ British Columbia, Dept Chem, Struct Chem Facil, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada in 2019.0, Cited 64.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

Indolizine derivatives are obtained by irradiation of 2-benzoyl-N-benzylpyridinium derivatives and dimethyl acetylene dicarboxylate, thus providing a competitive and complementary base- and catalyst-free synthesis. With this method, the first example of a crystallochromic indolizine is presented, whose color in the solid state depends on the out-of-plane torsion of the benzoyl substituent.

Safety of Phenyl(pyridin-2-yl)methanone. Welcome to talk about 91-02-1, If you have any questions, you can contact Dohmen, C; Ihmels, H; Kreienmeier, R; Patrick, BO or send Email.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Search for chemical structures by a sketch :91-02-1

SDS of cas: 91-02-1. Welcome to talk about 91-02-1, If you have any questions, you can contact Sun, YX; Li, XS; Yang, M; Xu, WT; Xie, J; Ding, MN or send Email.

SDS of cas: 91-02-1. In 2020 GREEN CHEM published article about AEROBIC OXIDATION; ANODIC-OXIDATION; ORGANIC ELECTROSYNTHESIS; N-HYDROXYPHTHALIMIDE; ELECTRON-TRANSFER; PRIMARY ALCOHOLS; REDOX CATALYSTS; P-XYLENE; EFFICIENT; HYDROCARBONS in [Sun, Yuxia; Li, Xiaoshan; Yang, Miao; Ding, Mengning] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem, Nanjing 210023, Peoples R China; [Xu, Wentao; Xie, Jin] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Coordinat Chem, Jiangsu Key Lab Adv Organ Mat, Nanjing 210023, Peoples R China in 2020, Cited 78. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

The selective oxidation of C-H bond is critical for feedstock manufacturing in chemical industry. Current strategies typically involve the use of oxygen or peroxide as the oxidation reagent under high temperature, which sets severe challenges in production sustainability and industrial safety. Herein, we demonstrate an environmental-friendly and safe electrocatalytic strategy for the selective oxidation of benzyl group to ketones at ambient conditions, while using water as the sole oxygen source. Water addition reduces the onset potential of anodic C-H oxidation, and produces 1-tetralone with satisfying conversion and excellent ketone to alcohol ratio. Layered MnO2 catalysts (with rich oxygen vacancies) further adjust the water affinity and facilitate the oxidation, leading to a significantly improved faradaic efficiency.

SDS of cas: 91-02-1. Welcome to talk about 91-02-1, If you have any questions, you can contact Sun, YX; Li, XS; Yang, M; Xu, WT; Xie, J; Ding, MN or send Email.

Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

What Kind of Chemistry Facts Are We Going to Learn About Phenyl(pyridin-2-yl)methanone

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Authors Zhong, J; Long, Y; Yan, XF; He, SY; Ye, RY; Xiang, HF; Zhou, XG in AMER CHEMICAL SOC published article about C-C BOND; CARBON-CARBON BONDS; CONJUGATED YNONES; ARYL KETONES; CLEAVAGE; PALLADIUM; DECARBONYLATION; REARRANGEMENT; FUNCTIONALIZATION; CARBOACYLATION in [Zhong, Jing; Long, Yang; Yan, Xufei; He, Shiyu; Ye, Runyou; Xiang, Haifeng; Zhou, Xiangge] Sichuan Univ, Coll Chem, 29 Wangjiang Rd, Chengdu 610064, Peoples R China in 2019, Cited 75. Recommanded Product: 91-02-1. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1

A rhodium-catalyzed Suzuki-Miyaura coupling reaction via C(O)-C bond activation to form 2-benzoylpyridine N-oxide derivatives is reported. Both the C(O)-C(sp(2)) and C(O)-C(sp(3)) bond could be activated during the reaction with yields up to 92%. The N-oxide moiety could be employed as a traceless directing group, leading to free pyridine ketones.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

What advice would you give a new faculty member or graduate student interested in a career Phenyl(pyridin-2-yl)methanone

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I found the field of Chemistry very interesting. Saw the article Synthesis, structural characterization, Hirshfeld surface analysis, antimicrobial activity, and DNA cleavage studies of (Z)-4-methyl-N ‘-(phenyl(pyridin-2-yl)methylene)benzenesulfonohydrazide and its Co(II), Ni(II) and Zn(II) complexes published in 2019.0. Recommanded Product: 91-02-1, Reprint Addresses Ataol, CY (corresponding author), Cankiri Karatekin Univ, Fac Sci, Dept Phys, TR-18100 Cankiri, Turkey.. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

The NNO tridentate Schiff base ligand of 2-benzoyl pyridine sulfonyl hydrazone (HL) and its transition metal complexes [CoL2] (1), [NiL2] (2) and [ZnL2] (3) have been synthesized and characterized by analytical and spectroscopic studies. The molecular structures of HL and [NiL2] (2) have been investigated by X-ray diffraction and DET/B3LYP methods. Based on the optimized structures, a single point energy calculation was made for HL and (2) in the different solvent media. The stability of the molecular structures was investigated in different solvent environments by calculating the molecular orbital energies and total energies of the molecular structures. The global reactivity parameters were obtained and the interactions between the molecules with DNA bases such as adenine, cytosine, guanine, and thymine were investigated by using the ECT (electrophilicity-based charge transfer) method and Delta N (charge transfer). Hirshfeld surfaces of HL and (2) complex were investigated and the interaction energies between the molecules participating in C-H center dot center dot center dot O/pi interactions in the molecular structures were calculated by using the CE-HF energy model. From elemental analysis data, the metal-ligand ratio of the complexes was found to be 1:2. All compounds were examined for their antimicrobial activity against pathogenic microorganisms by the well-diffusion method. DNA cleavage studies of compounds were screened by the agarose gel electrophoresis method. The results showed that complex (3) showed highly nicking activity, while HL, (1) and (2) complexes didn’t show any nicking activity. (C) 2019 Elsevier B.V. All rights reserved.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem

Interesting scientific research on Phenyl(pyridin-2-yl)methanone

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I found the field of Pharmacology & Pharmacy very interesting. Saw the article Novel [1,2,3] triazolo[1,5-a]pyridine derivatives are trypanocidal by sterol biosynthesis pathway alteration published in 2019. Recommanded Product: Phenyl(pyridin-2-yl)methanone, Reprint Addresses Maya, JD (corresponding author), Univ Chile, Fac Med, Inst Ciencias Biomed ICBM, Clin & Mol Pharmacol Program, Independencia 1027, Santiago 1027, Chile.. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

Aim: To study a new series of [1,2,3] triazolo[1,5-alpha] pyridine derivatives as trypanocidal agents because current antichagasic pharmacologic therapy is only partially effective. Materials & methods: The effect of the series upon Trypanosoma cruzi epimastigotes and murine macrophages viability, cell cycle, cell death and on the metabolites of the sterol biosynthesis pathway was measured; also, docking in 14 alpha-demethylase was analyzed. Results: Compound 16 inhibits 14 alpha-demethylase producing an imbalance in the cholesterol/ergosterol synthesis pathway, as suggested by a metabolic control and theoretical docking analysis. Consequently, it prevented cell proliferation, stopping the cellular cycle at the G2/M phase, inducing cell death. Conclusion: Although the exact cell death mechanism remained elusive, this series can be used for the further rational design of novel antiparasitic molecules.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem