1135-32-6 Usage
Description
1,2-BIS(2-PYRIDYL)ETHYLENE, with the molecular formula C14H12N2, is a bidentate ligand that plays a significant role in coordination chemistry and catalysis. Its distinctive structure facilitates the formation of stable complexes with a variety of metal ions, which is highly beneficial in both organic and inorganic synthesis. Moreover, this chemical compound has garnered interest for its potential applications in fluorescence sensing and imaging, as well as in the innovation of new materials and pharmaceuticals. The intriguing photophysical properties of 1,2-BIS(2-PYRIDYL)ETHYLENE, including its phosphorescence, broaden its potential applications across diverse scientific and industrial domains.
Uses
Used in Coordination Chemistry:
1,2-BIS(2-PYRIDYL)ETHYLENE is used as a bidentate ligand for the formation of stable complexes with metal ions, which is crucial in coordination chemistry for various applications, including the development of catalysts and the study of metal ion interactions.
Used in Catalysis:
As a ligand in catalytic processes, 1,2-BIS(2-PYRIDYL)ETHYLENE enhances the efficiency and selectivity of catalytic reactions, making it a valuable component in the design of homogeneous and heterogeneous catalysts.
Used in Fluorescence Sensing and Imaging:
1,2-BIS(2-PYRIDYL)ETHYLENE is utilized as a fluorescent probe or imaging agent due to its photophysical properties, allowing for the detection and visualization of specific targets or processes in biological and chemical systems.
Used in Pharmaceutical Development:
1,2-BIS(2-PYRIDYL)ETHYLENE serves as a potential building block or active ingredient in the development of new pharmaceuticals, leveraging its ability to form complexes with metal ions and its inherent fluorescence properties for targeted drug delivery or therapeutic applications.
Used in Material Science:
1,2-BIS(2-PYRIDYL)ETHYLENE is employed in the creation of new materials, such as organic light-emitting diodes (OLEDs) or sensors, where its phosphorescent properties can be harnessed to improve device performance or create novel material functionalities.
Used in Research and Development:
In academic and industrial research settings, 1,2-BIS(2-PYRIDYL)ETHYLENE is used as a model compound to study fundamental aspects of coordination chemistry, photophysics, and the development of new synthetic methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 1135-32-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1135-32:
(6*1)+(5*1)+(4*3)+(3*5)+(2*3)+(1*2)=46
46 % 10 = 6
So 1135-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N2/c1(11-3-7-13-8-4-11)2-12-5-9-14-10-6-12/h1-10H/b2-1-
1135-32-6Relevant articles and documents
Synthesis and properties of new electrochromic derivatives of 3-aryl-4,5-bis(pyridin-4-yl)oxazole
Chudov,Levchenko,Poroshin,Shchegol’kov,Shmelin,Grebennikov
, p. 1565 - 1569 (2019)
A series of new electrochromic derivatives of 3-aryl-4,5-bis(pyridin-4-yl)isoxazole was synthesized. Their electrochemical characteristics were studied by cyclic voltammetry, and a low eff ect of the substituents in the isoxazole and pyridinium cycles on the positions of the oxidation and reduction peaks was shown. The electrochromic cells prepared on the basis of the synthesized compounds were reversibly colored into brown upon the application of a voltage of 1.5 V. The spectral properties of the synthesized compounds under the electric field application and their stability for cycling from 0 to 2 V were studied.
Production of [...] (by machine translation)
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Paragraph 0045; 0047, (2019/06/07)
[A] can be obtained in a high yield production of cheap material and [...][...] of. (1) According to the reaction scheme represented by formula [a], (a)- (e) step without purification of intermediate products isolated formyl pyridine produced through a method. (A) a cyanopyridine, formyl pyridine (b) present in the acid and a metal catalyst under hydrogen added in the reaction liquid after hydrogenation steps (25 °C converted value) or more by neutralizing the formyl pyridine to produce free pH4 step (c) (d) was obtained by the extraction process of extracting the formyl pyridine in an organic solvent to produce formyl pyridine (e) concentrating the solution to a process for concentrating a formyl pyridine, methylpyridine using acid halide or acid anhydride with a condensation process[R′ and R " is H, an alkyl group, an aryl group, a heterocyclic group or a halogen atom][Drawing] no (by machine translation)
Synthesis and thermal oxidative degradation of quaternized 1,2-dipyridylethanes (-ethylenes) and their oxo derivatives
Chekryshkin,El'chisheva,Vnutskikh,Shklyaev
scheme or table, p. 1454 - 1460 (2011/03/17)
Quaternized compounds derived from 1,2-dipyridylethanes (-ethylenes) and their oxo derivatives were synthesized and characterized. Their thermal degradation was studied, and the dependence of the degradation sequence on the structure of the compounds was examined. Pleiades Publishing, Ltd., 2010.