Category: 91-02-1

Recommanded Product: 91-02-1. Danelli, P; Tsantis, ST; Kitos, A; Psycharis, V; Raptopoulou, CP; Tsipis, A; Perlepes, SP in [Danelli, Panagiota; Tsantis, Sokratis T.; Kitos, Alexandros; Perlepes, Spyros P.] Univ Patras, Dept Chem, Patras 26504, Greece; [Psycharis, Vassilis; Raptopoulou, Catherine P.] NCSR Demokritos, Inst Nanosci & Nanotechnol, Aghia Paraskevi 15310, Greece; [Tsipis, Athanassios] Univ Ioannina, Dept Chem, GR-45110 Ioannina, Greece published Investigating the isolation and interconversion of two diastereoisomers in an octahedral Ni(II)A(2)((BC)over-cap(2) system in 2019.0, Cited 23.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

Two diastereoisomers of bis(2-benzoylpyridine-O,N)dichloridonickel(II) have been isolated from the reactions of nickel(II) chloride hexahydrate and the organic ligand depending on the reaction solvent (ethanol, acetonitrile) used. DFT studies indicate that one of the isomers is more stable in both solvents, but nevertheless different diastereoisomers are crystallized from the two solvents. The two complexes represent the first pair of well characterized diastereoisomers in the coordination chemistry of 2-pyridyl ketones, providing a new example in the chemistry of octahedral MA(2)(BC) over cap (2) complexes (A = a monodentate ligand, (BC) over cap = an unsymmetrical bidentate chelate).

About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Danelli, P; Tsantis, ST; Kitos, A; Psycharis, V; Raptopoulou, CP; Tsipis, A; Perlepes, SP or concate me.. Recommanded Product: 91-02-1

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

An article Chirality-Economy Catalysis: Asymmetric Transfer Hydrogenation of Ketones by Ru-Catalysts of Minimal Stereogenicity WOS:000471212600085 published article about ENANTIOSELECTIVE TRANSFER HYDROGENATION; LIGAND BIFUNCTIONAL CATALYSIS; ACHIRAL BENZOPHENONE LIGAND; RUTHENIUM(II) COMPLEXES; AROMATIC KETONES; DIAMINE; REDUCTION; MECHANISM; ALCOHOLS; NETWORK in [Chen, Fumin; He, Dongxu; Chang, Xiaoyong; Xu, Chen; Xing, Xiangyou] Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China; [Chen, Fumin; He, Dongxu; Chang, Xiaoyong; Xu, Chen; Xing, Xiangyou] Southern Univ Sci & Technol, Dept Chem, Shenzhen 518055, Peoples R China; [Chen, Li; Wang, David Zhigang] Peking Univ, Shenzhen Grad Sch, Sch Chem Biol & Biotechnol, Shenzhen 518055, Peoples R China; [Chen, Li] Danzao Subbur Adm Social Insurance Fund Fushan Na, Foshan 528216, Peoples R China; [Wang, David Zhigang] Shenzhen UV ChemTech, Shenzhen 518057, Peoples R China in 2019.0, Cited 36.0. Product Details of 91-02-1. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1

This manuscript describes the design and synthesis of Ru catalysts that feature only a single stereogenic element, yet this minimal chirality resource is demonstrated to be competent for effecting high levels of stereoinduction in the asymmetric transfer hydrogenation over a broad range of ketone substrates, including those that are not accommodated by known catalyst systems. The single stereogenic center of the (1-pyridine-2-yl)methanamine) is the only point-chirality in the catalysts, which simplifies this catalyst system relative to existing literature protocols.

About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Chen, FM; He, DX; Chen, L; Chang, XY; Wang, DZ; Xu, C; Xing, XY or concate me.. Product Details of 91-02-1

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

Recently I am researching about HETEROPOLYTUNGSTATE DERIVATIVES; HETEROGENEOUS CATALYSTS; CYCLOHEXANE OXIDATION; W-183 NMR; METAL; KEGGIN; PERFORMANCE; FUNCTIONALIZATION; HYDROCARBONS; OXYGENATION, Saw an article supported by the Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [21571050, 21573056, 21771053, 21771054]; 2019 Student Innovative Pilot Plan of Henan University [201910475079]. Formula: C12H9NO. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Ma, XY; Wang, P; Liu, ZH; Xin, CH; Wang, SY; Jia, JG; Ma, PT; Niu, JY; Wang, JP. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

POM-supported metal carbonyl derivatives (PMCDs) represent a family of tremendous potential catalysts owing to their peculiar physical and chemical properties. Yet low-valence transition metal-substituted Dawson-type PMCD catalysts are uncommon. Hence, we synthesized a tricobalt-substituted PMCDs by conventional aqueous solution method, [Na(H2O)(5)](NH4)(7)[P2W15O56Co3(H2O)(3)(OH)(3)Re(CO)(3)]center dot 13H(2)O (1), and characterized by single crystal X-ray diffraction crystallography, IR, and thermogravimetric analyses (TGA), etc. The obtained compound 1 was employed as a catalyst for the oxidation of diphenylmethane (DPM) to benzophenone, giving 96.8% yield in the presence of tert-butyl hydroperoxide (TBHP) and pyridine. The control experiments indicate that Co metal ion plays an important role in the catalytic reactions. As a side note, the electrospray ionization mass spectrometry (ESI-MS) and UV spectroscopy showed that 1 can retain its integrity in solution, and magnetic measurements indicated that 1 exhibited a weaker ferromagnetic interaction at low temperature.

Formula: C12H9NO. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Ma, XY; Wang, P; Liu, ZH; Xin, CH; Wang, SY; Jia, JG; Ma, PT; Niu, JY; Wang, JP or concate me.

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

Product Details of 91-02-1. Authors Liu, YH; Yu, Y; Sun, CY; Fu, YW; Mang, ZG; Shi, L; Li, H in AMER CHEMICAL SOC published article about in [Liu, Yonghai; Yu, Yang; Sun, Chengyu; Fu, Yiwei; Mang, Zhiguo; Li, Hao] East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China; [Liu, Yonghai; Yu, Yang; Sun, Chengyu; Fu, Yiwei; Mang, Zhiguo; Li, Hao] East China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China; [Shi, Lei] Firmenich Aromat China Co Ltd, Corp R&D Div, Shanghai 201108, Peoples R China in 2020.0, Cited 48.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1

We developed an approach for direct selective hydroxylation of heterobenzylic methylenes to secondary alcohols avoiding overoxidation to ketones by using a KOBu-t/DMSO/air system. Most reactions could reach completion in several minutes to give hydroxylated products in 41-76% yields. Using DMSO-d(6), this protocol resulted in difunctionalization of heterobenzylic methylenes to afford a-deuterated secondary alcohols (>93% incorporation). By employing this method, active pharmaceutical ingredients carbinoxamine and doxylamine were synthesized in two steps in moderate yields.

About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Liu, YH; Yu, Y; Sun, CY; Fu, YW; Mang, ZG; Shi, L; Li, H or concate me.. Product Details of 91-02-1

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

An article Electrochemical Synthesis of [1,2,3]Triazolo[1,5-a]pyridines through Dehydrogenative Cyclization WOS:000481928500015 published article about C-H FUNCTIONALIZATION; CATALYZED TRANSANNULATION; EFFICIENT SYNTHESIS; COUPLING REACTIONS; PYRIDOTRIAZOLES; METAL; STRATEGIES; HYDRAZONES; OXIDATION; PYRIDINES in [Xu, Pin; Xu, Hai-Chao] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Coll Chem & Chem Engn, Xiamen 361005, Fujian, Peoples R China in 2019.0, Cited 61.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1. Safety of Phenyl(pyridin-2-yl)methanone

The synthesis of [1,2,3]triazolo[1,5-a]pyridines through electrochemical dehydrogenative cyclization of hydrazones of 2-acylpyridines is presented. The reactions are carried out under mild conditions without oxidizing reagents or transition-metal catalysts.

Safety of Phenyl(pyridin-2-yl)methanone. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Xu, P; Xu, HC or concate me.

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

Recently I am researching about HORIUTI-POLANYI MECHANISM; STABILIZED PALLADIUM NANOPARTICLES; COPD BIOMARKER DESMOSINE; HETEROGENEOUS CATALYSIS; CARBOXYLIC-ACIDS; IONIC LIQUIDS; AMINES; WATER; HYDRODEHALOGENATION; TRANSFORMATION, Saw an article supported by the JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [JP17K01953, JP20K05734]. Name: Phenyl(pyridin-2-yl)methanone. Published in WILEY-V C H VERLAG GMBH in WEINHEIM ,Authors: Tanaka, N; Usuki, T. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

Hydrogenation of over a dozen aromatic compounds, including both heteroarenes and arenes, over palladium on carbon (Pd/C, 1-100 mol%) with H-2-balloon pressure at room temperature is reported. Analyses using pyridine as a model substrate revealed that acetic acid was the best solvent, as using only 1 mol% Pd/C provided piperidine quantitatively. Substrate scope analysis and density functional theory calculations indicated that reaction rates are highly dependent on frontier molecular orbital characteristics and the steric bulkiness of substituents. Moreover, the established method was used for the concise synthesis of the anti-Alzheimer drug donepezil (Aricept (R)).

Name: Phenyl(pyridin-2-yl)methanone. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Tanaka, N; Usuki, T or concate me.

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

Recently I am researching about PROTEIN; AGONISTS; LIGANDS; ANAPHYLATOXINS; REGULATORS; C5A, Saw an article supported by the National Health and Medical Research CouncilNational Health and Medical Research Council of Australia [1145372, 1084018, 1028423]; Australian Research CouncilAustralian Research Council [DP130100629, DP180103244]; Australian Research Council Centre of Excellence in Advanced Molecular ImagingAustralian Research Council [CE140100011]; Queensland Government (CIF grant); University of QueenslandUniversity of Queensland; UQ Postdoctoral Research Fellowship; [1027369]; [1117017]. Product Details of 91-02-1. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Rowley, JA; Reid, RC; Poon, EKY; Wu, KC; Lim, JX; Lohman, RJ; Hamidon, JK; Yau, MK; Halili, MA; Durek, T; Iyer, A; Fairlie, DP. The CAS is 91-02-1. Through research, I have a further understanding and discovery of Phenyl(pyridin-2-yl)methanone

Structure-activity relationships for a series of small-molecule thiophenes resulted in potent and selective antagonism of human Complement C3a receptor. The compounds are about 100-fold more potent than the most reported antagonist SB290157. A new compound JR14a was among the most potent of the new antagonists in vitro, assessed by (a) inhibition of intracellular calcium release (IC50 10 nM) induced in human monocyte-derived macrophages by 100 nM C3a, (b) inhibition of beta-hexosaminidase secretion (IC50 8 nM) from human LAD2 mast cells degranulated by 100 nM C3a, and (c) selectivity for human C3aR over C5aR JR14a was metabolically stable in rat plasma and in rat liver microsomes and efficacious in rats when given orally to suppress rat paw inflammation, macrophage and mast cell activation, and histopathology induced by intraplantar paw administration of a C3aR agonist. Potent C3aR antagonists are now available for interrogating C3a receptor activation and suppressing C3aR-mediated inflammation in mammalian physiology and disease.

Product Details of 91-02-1. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Rowley, JA; Reid, RC; Poon, EKY; Wu, KC; Lim, JX; Lohman, RJ; Hamidon, JK; Yau, MK; Halili, MA; Durek, T; Iyer, A; Fairlie, DP or concate me.

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

Yu, T; Guo, MQ; Wen, SMM; Zhao, RR; Wang, JL; Sun, YL; Liu, QX; Zhou, HF in [Yu, Tao; Guo, Mingqing; Wen, Simiaomiao; Zhao, Rongrong; Wang, Jinlong; Sun, Yanli; Liu, Qixing; Zhou, Haifeng] China Three Gorges Univ, Res Ctr Green Pharmaceut Technol & Proc, Hubei Key Lab Nat Prod Res & Dev, Coll Biol & Pharmaceut Sci, Yichang 443002, Peoples R China published Poly(ethylene glycol) dimethyl ether mediated oxidative scission of aromatic olefins to carbonyl compounds by molecular oxygen in 2021, Cited 51. Computed Properties of C12H9NO. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1.

A simple, and practical oxidative scission of aromatic olefins to carbonyl compounds using O-2 as the sole oxidant with poly(ethylene glycol) dimethyl ether as a benign solvent has been developed. A wide range of monosubstituted, gem-disubstituted, 1,2-disubstituted, trisubstituted and tetrasubstituted aromatic olefins was successfully converted into the corresponding aldehydes and ketones in excellent yields even with gram-scale reaction. Some control experiments were also conducted to support a possible reaction pathway.

Computed Properties of C12H9NO. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Yu, T; Guo, MQ; Wen, SMM; Zhao, RR; Wang, JL; Sun, YL; Liu, QX; Zhou, HF or concate me.

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

An article Structurally characterized mononuclear isostructural Ni(II), Cu(II) and Zn (II) complexes as a functional model for phenoxazinone synthase activity WOS:000499768700046 published article about COBALT(III) COMPLEX; CATECHOLASE; OXIDATION; DIOXYGEN; LIGAND; EXAMPLE in [Chatterjee, Arnab; Ghosh, Rajarshi] Univ Burdwan, Dept Chem, Burdwan 713104, W Bengal, India; [Khan, Sumitava] Burdwan Raj Coll, Dept Chem, Burdwan 713104, W Bengal, India in 2019.0, Cited 32.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1. Application In Synthesis of Phenyl(pyridin-2-yl)methanone

Three new mononuclear complexes of the type [M(L)(2)](ClO4)(2), with Ni(II) (1), Cu(II) (2) and Zn(II) (3) ions, have been synthesized and structurally characterized, using the N,N,O donor Schiff base ligand 2-[(phenyl-pyridine-2-yl-methylene)-amino]-ethanol]. An X-ray diffraction study reveals identical crystallization patterns for each of the complexes, in the monoclinic crystal system with the C2/c space group. Interestingly, the synthesized complexes are isostructural in nature. The complexes showed biomimetic phenoxazinone synthase-like activity for the aerial oxidation of o-aminophenol to phenoxazine-2-one, separately in methanol (MeOH) and acetonitrile (ACN) solutions. For each of the complexes, the turnover numbers were found to be higher in MeOH than in ACN. The highest catalytic activity between among the three complexes was found to be for complex 2. (C) 2019 Elsevier Ltd. All rights reserved.

Application In Synthesis of Phenyl(pyridin-2-yl)methanone. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Chatterjee, A; Khan, S; Ghosh, R or concate me.

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

HPLC of Formula: C12H9NO. Authors Kim, JH; Ofori, S; Parkin, S; Vekaria, H; Sullivan, PG; Awuah, SG in ROYAL SOC CHEMISTRY published article about in [Kim, Jong Hyun; Ofori, Samuel; Parkin, Sean; Awuah, Samuel G.] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA; [Awuah, Samuel G.] Univ Kentucky, Coll Pharm, Ctr Pharmaceut Res & Innovat, Lexington, KY 40536 USA; [Awuah, Samuel G.] Univ Kentucky, Coll Pharm, Dept Pharmaceut Sci, Lexington, KY 40536 USA; [Vekaria, Hemendra; Sullivan, Patrick G.] Univ Kentucky, Spinal Cord & Brain Injury Res Ctr, Lexington, KY USA; [Sullivan, Patrick G.] Univ Kentucky, Dept Neurosci, Lexington, KY USA; [Sullivan, Patrick G.] Lexington Vet Affairs Healthcare Syst, Lexington, KY USA in 2021.0, Cited 75.0. The Name is Phenyl(pyridin-2-yl)methanone. Through research, I have a further understanding and discovery of 91-02-1

Expanding the chemical diversity of metal complexes provides a robust platform to generate functional bioactive reagents. To access an excellent repository of metal-based compounds for probe/drug discovery, we capitalized on the rich chemistry of gold to create organometallic gold(III) compounds by ligand tuning. We obtained novel organogold(III) compounds bearing a 1,2-bis(diphenylphosphino)benzene ligand, providing structural diversity with optimal physiological stability. Biological evaluation of the lead compound AuPhos-89 demonstrates mitochondrial complex I-mediated alteration of the mitochondrial electron transport chain (ETC) to drive respiration and diminish cellular energy in the form of adenosine triphosphate (ATP). Mechanism-of-action efforts, RNA-Seq, quantitative proteomics, and NCI-60 screening reveal a highly potent anticancer agent that modulates mitochondrial ETC. AuPhos-89 inhibits the tumor growth of metastatic triple negative breast cancer and represents a new strategy to study the modulation of mitochondrial respiration for the treatment of aggressive cancer and other disease states where mitochondria play a pivotal role in the pathobiology.

HPLC of Formula: C12H9NO. About Phenyl(pyridin-2-yl)methanone, If you have any questions, you can contact Kim, JH; Ofori, S; Parkin, S; Vekaria, H; Sullivan, PG; Awuah, SG or concate me.

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