78500-89-7 Usage
Uses
Used in Organic Synthesis:
2,6-diphenyl-4-broMo-pyridine is used as a ligand for transition metal catalysts in organic synthesis. Its ability to form stable complexes with metals like iron, ruthenium, and palladium enhances the efficiency and selectivity of various catalytic reactions.
Used in Catalytic Reactions:
In the field of catalysis, 2,6-diphenyl-4-broMo-pyridine is used as a ligand to facilitate cross-coupling, hydrogenation, and oxidation reactions. The complexes formed with transition metals have been extensively studied for their catalytic properties, offering improved reaction rates and selectivity in various chemical processes.
Used in Material Science:
2,6-diphenyl-4-broMo-pyridine has shown potential for use in material science, particularly in the development of luminescent compounds. Its application in the creation of organic light-emitting diodes (OLEDs) and other optoelectronic devices is driven by its ability to enhance the performance and efficiency of these technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 78500-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,0 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 78500-89:
(7*7)+(6*8)+(5*5)+(4*0)+(3*0)+(2*8)+(1*9)=147
147 % 10 = 7
So 78500-89-7 is a valid CAS Registry Number.
78500-89-7Relevant academic research and scientific papers
Intramolecular Nitrene Insertions into Aromatic and Heteroaromatic Systems. Part 7. Insertions into Electron-deficient Rings
Carde, Robert N.,Hayes, Peter C.,Jones, Gurnos,Cliff, Cynthya J.
, p. 1132 - 1142 (2007/10/02)
A number of routes to o-aminotriphenylmethanes are described, where one benzene ring, or both, carry potential ester groups.The most useful synthon is shown to be the 1,3-dioxan-2-yl substituent, and using this methyl 2-aminodiphenylmethane-4'-carboxylate (18) and dimethyl 2-aminotriphenylmethane-4',4''-dicarboxylate (28) have been prepared.The azides from these, respectively (19) and (29), on thermolysis at 200 deg C gave azepinoindoles (48) and (51), the first examples of ring expansion by an arylnitrene of benzene rings with electron-withdrawing substituents.Also reported are syntheses of 3- and 4-(2-azidobenzyl)pyridines (38) and (39), and of 2-(2-azidobenzyl)thiazole (40); decomposition of these azides gave mainly polymers.
