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Trifluoro-methanesulfonic acid 4'''-methyl-[1,1';2',1'';2'',1''']quaterphenyl-2-yl ester is a chemical compound derived from quaterphenyl, a polycyclic aromatic hydrocarbon. It is characterized by its strong acidity, high stability, and solubility in polar organic solvents, making it a valuable reagent in organic synthesis reactions and a catalyst in various chemical processes.

882971-91-7

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882971-91-7 Usage

Uses

Used in Organic Synthesis:
Trifluoro-methanesulfonic acid 4'''-methyl-[1,1';2',1'';2'',1''']quaterphenyl-2-yl ester is used as a reagent in organic synthesis for its strong acidity and catalytic properties, facilitating various chemical reactions and the formation of desired products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, trifluoro-methanesulfonic acid 4'''-methyl-[1,1';2',1'';2'',1''']quaterphenyl-2-yl ester is utilized as a key intermediate in the synthesis of certain drugs, contributing to the development of novel therapeutic agents.
Used in Materials Science:
trifluoro-methanesulfonic acid 4'''-methyl-[1,1';2',1'';2'',1''']quaterphenyl-2-yl ester is employed in materials science for its potential applications in the creation of advanced materials with unique properties, such as high thermal stability and electrical conductivity.
Used in Chemical Research:
Trifluoro-methanesulfonic acid 4'''-methyl-[1,1';2',1'';2'',1''']quaterphenyl-2-yl ester serves as a valuable tool in chemical research, enabling scientists to explore new reaction mechanisms, develop innovative synthetic methods, and gain insights into the fundamental aspects of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 882971-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,9,7 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 882971-91:
(8*8)+(7*8)+(6*2)+(5*9)+(4*7)+(3*1)+(2*9)+(1*1)=227
227 % 10 = 7
So 882971-91-7 is a valid CAS Registry Number.

882971-91-7Downstream Products

882971-91-7Relevant academic research and scientific papers

Repetitive two-step method for oligoarene synthesis through rapid cross-coupling of hydroxyphenylboronic acids and anhydrides

Ishikawa, Shunpei,Manabe, Kei

, p. 164 - 165 (2007/10/03)

A two-step Suzuki-Miyaura coupling-Inflation procedure, which features the use of hydroxyphenylboronic acids or anhydrides in the palladium-catalyzed cross-coupling step, has been developed for the synthesis of oligoarenes. Copyright

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