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2-(4-fluorophenyl)-5-fluoropyridine is a heterocyclic aromatic compound with the molecular formula C11H7FN2. It features a fluorine-substituted phenyl ring and a fluorine-substituted pyridine ring, contributing to its potential biological activities and applications in pharmaceutical and agrochemical synthesis.

511522-71-7

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511522-71-7 Usage

Uses

Used in Pharmaceutical Industry:
2-(4-fluorophenyl)-5-fluoropyridine is used as a building block for the synthesis of pharmaceutical products due to its potential biological activities, such as antitumor and anti-inflammatory properties. The presence of fluorine atoms in its structure enhances its chemical stability and interaction with biological targets, making it a valuable tool for drug discovery and development.
Used in Agrochemical Industry:
2-(4-fluorophenyl)-5-fluoropyridine is used as a building block for the synthesis of agrochemical products. Its chemical properties and potential biological activities make it a useful compound in the development of new agrochemicals, potentially improving crop protection and yield.

Check Digit Verification of cas no

The CAS Registry Mumber 511522-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,1,1,5,2 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 511522-71:
(8*5)+(7*1)+(6*1)+(5*5)+(4*2)+(3*2)+(2*7)+(1*1)=107
107 % 10 = 7
So 511522-71-7 is a valid CAS Registry Number.

511522-71-7Downstream Products

511522-71-7Relevant academic research and scientific papers

Effects of fluorine substituent on properties of cyclometalated iridium(III) complexes with a 2,2′-bipyridine ancillary ligand

Chen, Yan,Liu, Chun,Wang, Lei

, (2019)

Cationic cyclometalated Ir(III) complexes (Ir1-Ir5) with fluorine-substituted 2-phenylpyridine (ppy) derivatives as C^N cyclometalating ligands and 2,2′-bipyridine (bpy) as the ancillary ligand, have been synthesized and fully characterized. The influences of the number and the position of fluorine atoms at the cyclometalating ligands on the photophysical, electrochemical and oxygen sensing properties of the Ir(III) complexes have been investigated systematically. The introduction of fluorine on the C^N cyclometalating ligands of the complexes results in blue-shifts of the maximum emission wavelengths, and increases in the photoluminescence quantum yields (ΦPL), phosphorescence lifetimes and energy gaps, compared to the non-fluorinated [Ir(ppy)2(bpy)]+PF6? (Ir0). Among them, 2-(2,4-difluorophenyl)pyridine-derived Ir4 shows the maximum blue-shift (514 nm vs. 575 nm for Ir0) and the highest ΦPL (50.8% vs. 6.5% for Ir0). The complex Ir3 with 2-(4-fluorophenyl)-5-fluoropyridine as C^N ligand exhibits the highest oxygen sensitivity and excellent operational stability in 10 cycles within 4000 s.

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