20357-70-4 Usage
Uses
Used in Research and Development Applications:
2-Methoxydibenzofuran, 96 is utilized as a chemical compound in various research and development applications. Its unique structure and properties make it a valuable component in the synthesis of new compounds and the study of chemical reactions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Methoxydibenzofuran, 96 is used as a starting material or intermediate in the synthesis of various drug molecules. Its presence in the final product may vary depending on the specific synthesis process and the desired outcome.
Used in Chemical Synthesis:
2-Methoxydibenzofuran, 96 is employed as a key component in the synthesis of complex organic compounds. Its reactivity and structural features contribute to the formation of new molecules with potential applications in various fields, such as materials science, agrochemistry, and specialty chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 20357-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,5 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20357-70:
(7*2)+(6*0)+(5*3)+(4*5)+(3*7)+(2*7)+(1*0)=84
84 % 10 = 4
So 20357-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O2/c1-14-9-6-7-13-11(8-9)10-4-2-3-5-12(10)15-13/h2-8H,1H3
20357-70-4Relevant academic research and scientific papers
TRANSITION METAL CATALYSTS FOR C-O HYDROGENOLYSIS AND HYDRODEOXYGENATION
-
Paragraph 0175; 0176; 0177, (2014/07/08)
Phosphoranimide-metal catalysts and their role in C—O bond hydrogenolysis and hydrodeoxygenation (HDO) are disclosed. The catalysts comprise of first row transition metals such as nickel, cobalt and iron. The catalysts have a metal to anionic phosphoranimide ratio of 1:1 and catalyze C—O bond hydrogenolyses of a range of oxygen-containing organic compounds under lower temperature and pressure conditions than those commonly used in industrial hydrodeoxygenation.
Nickel-catalyzed intramolecular C-H arylation using aryl pivalates as electrophiles
Wang, Jiayi,Ferguson, Devin M.,Kalyani, Dipannita
, p. 5780 - 5790 (2013/07/19)
This paper describes a method for nickel catalyzed intramolecular C-H arylation using aryl pivalates as electrophiles. The transformation is efficient for the synthesis of diverse electronically and sterically differentiated dibenzofurans. Additionally, the method could be expanded toward the synthesis of carbazoles. Preliminary mechanistic studies of the transformation are also described.
