113710-69-3 Usage
Uses
Used in Organic Synthesis:
[1,1':3',1''-Terphenyl]-5'-carboxylic acid, 4'-benzoylis used as a building block in organic synthesis for its unique molecular structure and reactivity, allowing the creation of more complex molecules.
Used in Materials Science:
In the field of materials science, [1,1':3',1''-Terphenyl]-5'-carboxylic acid, 4'-benzoylis used as a component in the development of organic electronic materials, dyes, and pharmaceutical intermediates due to its specific properties and potential applications.
Used in Pharmaceutical Industry:
[1,1':3',1''-Terphenyl]-5'-carboxylic acid, 4'-benzoylis used as a pharmaceutical intermediate for its potential role in the development of new drugs and therapeutic agents.
Used in Dye Industry:
In the dye industry, [1,1':3',1''-Terphenyl]-5'-carboxylic acid, 4'-benzoylis used as a component in the creation of new dyes, taking advantage of its unique molecular structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 113710-69-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,1 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 113710-69:
(8*1)+(7*1)+(6*3)+(5*7)+(4*1)+(3*0)+(2*6)+(1*9)=93
93 % 10 = 3
So 113710-69-3 is a valid CAS Registry Number.
113710-69-3Relevant academic research and scientific papers
Pyrylium Compounds. 36. Substituted Benzoic Acid Esters from 2,4,6-Triarylpyrylium Salts and α-Ketocarboxylic Acid Esters
Zimmermann, Thomas,Fischer, Gerhard W.
, p. 499 - 510 (2007/10/02)
2,4,6-Triarylpyrylium salts 1 react with α-ketocarboxylic acid esters 2 in the presence of two equivalents of an appropriate condensing agent (e.g. dialkylamine salts of weak acids, triethylamine/acetic acid, or sodium acetate) to give 2-aroyl-3,5-diarylbenzoic acid esters 3.However, using only one equivalent of the condensing agent, the formation of 3,5-diarylbenzoic acid esters 5 predominates.Alkaline saponification of the new esters 3 and 5 yields the corresponding substituted benzoic acids 4 and 6, respectively. - I.r., u.v., n.m.r. and mass spectroscopic data of the novel products 3-6 are reported.
