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5-fluoro-2-(4-methylphenyl)pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1198348-26-3

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1198348-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1198348-26-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,3,4 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1198348-26:
(9*1)+(8*1)+(7*9)+(6*8)+(5*3)+(4*4)+(3*8)+(2*2)+(1*6)=193
193 % 10 = 3
So 1198348-26-3 is a valid CAS Registry Number.

1198348-26-3Relevant academic research and scientific papers

A general and highly efficient method for the construction of aryl-substituted N-heteroarenes

Liu, Chun,Han, Na,Song, Xiaoxiao,Qiu, Jieshan

, p. 5548 - 5551 (2010)

A general, simple and highly efficient method has been developed for the Pd(OAc)2-catalyzed ligand-free and aerobic Suzuki reaction of N-heteroaryl halides, which is strongly dependent on the molecular structure of solvent. A general, simple and highly efficient method has been developed for the Pd(OAc)2-catalyzed ligand-free and aerobic Suzuki reaction of N-heteroaryl halides including 2-pyridyl bromides, 3-pyridyl bromides, 3-quinolyl bromides, 5-pyrimidyl bromides and 2-pyrazyl chloride, which is strongly dependent on the molecular structure of solvent.

A general palladium-catalyzed cross-coupling of aryl fluorides and organotitanium (IV) reagents

He, Xiao-Yun

, p. 823 - 832 (2021/07/19)

Pd(OAc)2/1-[2-(di-tert-butylphosphanyl)phenyl]-4-methoxy-piperidine was demonstrated to effectively catalyze cross-coupling of aryl fluoride and aryl(alkyl) titanium reagent. Both electron-deficient and electron-rich aryl fluoride can react effectively with nucleophile and provide extensive functional groups tolerance. 2-Arylated product was realized by selective activation of the C–F bond. Graphic abstract: [Figure not available: see fulltext.].

Evaluation of Improved Glycogen Synthase Kinase-3α Inhibitors in Models of Acute Myeloid Leukemia

Neumann, Theresa,Benajiba, Lina,G?ring, Stefan,Stegmaier, Kimberly,Schmidt, Boris

, p. 8907 - 8919 (2015/12/09)

The challenge for glycogen synthase kinase-3 (GSK-3) inhibitor design lies in achieving high selectivity for one isoform over the other. The therapy of certain diseases, such as acute myeloid leukemia (AML), may require α-isoform specific targeting. The s

Systematic evaluation of HOMO energy levels for efficient dye regeneration in dye-sensitized solar cells

Funaki, Takashi,Otsuka, Hiromi,Onozawa-Komatsuzaki, Nobuko,Kasuga, Kazuyuki,Sayama, Kazuhiro,Sugihara, Hideki

supporting information, p. 15945 - 15951 (2015/03/03)

Thirty ruthenium complexes of the types [Ru(tctpy)(C^N)NCS] and [Ru(tctpy)(N^O)NCS] (C^N = cyclometalating ligand and N^O = pyridinecarboxylate and its derivatives) were synthesized and evaluated to identify the highest occupied molecular orbital (HOMO) energy level (EHOMO) for efficient dye regeneration in dye-sensitized solar cells. EHOMOof these complexes was systematically tuned by changing the electron-donating ability of the C^N and N^O ligands. For complexes with an EHOMOin the potential range more negative than 0.5 V vs. a saturated calomel electrode (SCE), the incident photon-to-current conversion efficiency (IPCE) increased with a positive shift in EHOMObut could not exceed 70%, suggesting that rapid dye regeneration is difficult. On the other hand, high IPCEs above 70% were often observed for complexes with an EHOMOmore positive than 0.5 V vs. SCE. It is thus concluded that there is a threshold for efficient electron transfer near 0.5 V vs. SCE (ΔG2≈ 0.3 eV) for the series of these sensitizers. This journal is

A fast and oxygen-promoted protocol for the ligand-free Suzuki reaction of 2-halogenated pyridines in aqueous media

Liu, Chun,Yang, Weibo

supporting information; experimental part, p. 6267 - 6269 (2010/02/16)

A fast protocol has been developed for the construction of 2-aryl-substituted pyridine derivatives by the oxygen-promoted, ligand-free, Pd(OAc)2-catalyzed Suzuki reaction of 2-halogenated pyridines in aqueous isopropanol.

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