142946-80-3 Usage
Description
5-(trifluoromethyl)-2-[5-(trifluoromethyl)pyridin-2-yl]pyridine is a complex organic compound characterized by its trifluoromethyl and pyridine groups. It is a derivative of bipyridine, featuring a unique arrangement of fluorine atoms and pyridine rings that contribute to its chemical properties and potential applications.
Uses
Used in Photocatalysis:
5-(trifluoromethyl)-2-[5-(trifluoromethyl)pyridin-2-yl]pyridine is used as a ligand for the preparation of Ir(III) photocatalysts. Its unique structure and electronic properties make it suitable for enhancing the performance of these catalysts in various photocatalytic reactions, such as water splitting and organic synthesis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-(trifluoromethyl)-2-[5-(trifluoromethyl)pyridin-2-yl]pyridine may be utilized as a building block or intermediate for the synthesis of novel drugs targeting specific biological receptors or enzymes. Its structural diversity and potential for modification make it a valuable candidate for drug discovery and development.
Used in Chemical Synthesis:
5-(trifluoromethyl)-2-[5-(trifluoromethyl)pyridin-2-yl]pyridine can also be employed as a versatile intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and advanced materials. Its unique combination of fluorine and nitrogen atoms provides opportunities for further functionalization and diversification in chemical synthesis.
Used in Materials Science:
The compound may find applications in the field of materials science, where its electronic and structural properties could be exploited to develop new materials with specific properties, such as improved conductivity, stability, or optical characteristics.
Used in Analytical Chemistry:
5-(trifluoromethyl)-2-[5-(trifluoromethyl)pyridin-2-yl]pyridine could be utilized as a reagent or reference compound in analytical chemistry for the detection, quantification, or separation of various substances due to its distinct chemical and physical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 142946-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,9,4 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 142946-80:
(8*1)+(7*4)+(6*2)+(5*9)+(4*4)+(3*6)+(2*8)+(1*0)=143
143 % 10 = 3
So 142946-80-3 is a valid CAS Registry Number.
142946-80-3Relevant articles and documents
Modified Ullmann coupling of 2-chloro-3-trifluoromethylpyridine
Munavalli, S.,Rossman, D. I.,Szafraniec, L. L.,Beaudry, W. T.,Rohrbaugh, D. K.,et al.
, p. 1 - 6 (2007/10/02)
The application of the modified Ullmann reaction to 2-chloro-3-trifluoromethylpyridine furnishes 5,5'-bis(trifluoromethyl)-2,2'-bipyridine as the primary product, accompanied by small amounts of the expected 3,3'-bis(trifluoromethyl)-2,2'-bipyridine, 2-benzyl-3-(trifluoromethyl)pyridine, bibenzyl, 3-trifluoromethylpyridine, 3-methylpyridine, 2-hydroxyethyl-(3-trifluoromethylpyridyl) ether and 2-hydroxyethyl-(3-methylpyridyl) ether.For comparison purposes, a sample of 3,3'-bis-(trifluoromethyl)-2,2'-bipyridyl was prepared by the treatment of 2,2'-bipyridyl-3,3'-dicarboxylic acid with sulfur tetrafluoride.The formation of all but two compounds mentioned above can be rationalized on the basis of the single-electron-transfer process. - Keywords: Ullman coupling; Chlorotrifluoromethylpyridine; Bis(trifluoromethyl)bipyridine; Synthesis; NMR spectroscopy; Mass spectrometry
