6390-59-6 Usage
Description
[1,1'-Biphenyl]-2,2'-diol, 3,3'-bis(1,1-dimethylethyl)-5,5'-dimethylis a chemical compound characterized by its molecular formula C26H34O2. It is a type of diol, which means it contains two hydroxyl (OH) functional groups. [1,1'-Biphenyl]-2,2'-diol, 3,3'-bis(1,1-dimethylethyl)-5,5'-dimethylis also known as 3,3'-bis(tert-butyl)-5,5'-dimethyl-1,1'-biphenyl-2,2'-diol and is recognized for its high stability and ability to prevent chemical degradation.
Uses
Used in Plastics and Rubber Industry:
[1,1'-Biphenyl]-2,2'-diol, 3,3'-bis(1,1-dimethylethyl)-5,5'-dimethylis used as an antioxidant and stabilizer for enhancing the durability and longevity of various industrial and consumer products. Its application in this industry is due to its ability to prevent chemical degradation and maintain the integrity of materials exposed to harsh environmental conditions.
Used in Pharmaceutical Research:
[1,1'-Biphenyl]-2,2'-diol, 3,3'-bis(1,1-dimethylethyl)-5,5'-dimethylis also being studied for its potential pharmaceutical applications, particularly in the development of new drugs for the treatment of various medical conditions. The exploration of its pharmaceutical potential is driven by its unique chemical structure and the possibility of it interacting with biological systems in beneficial ways.
Check Digit Verification of cas no
The CAS Registry Mumber 6390-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6390-59:
(6*6)+(5*3)+(4*9)+(3*0)+(2*5)+(1*9)=106
106 % 10 = 6
So 6390-59-6 is a valid CAS Registry Number.
6390-59-6Relevant articles and documents
Oxidative photocatalytic homo- And cross-coupling of phenols: Nonenzymatic, catalytic method for coupling tyrosine
Niederer, Kyle A.,Gilmartin, Philip H.,Kozlowski, Marisa C.
, p. 14615 - 14623 (2020/12/23)
An oxidative photocatalytic method for phenol? phenol homo- and cross-coupling is described, and isolated yields of 16?97% are obtained. Measured oxidation potentials and computed nucleophilicity parameters support a mechanism of nucleophilic attack of one partner onto the oxidized neutral radical form of the other partner. Our understanding of this model permitted the development of cross-coupling reactions between nucleophilic phenols/arenes and easily oxidized phenols with high selectivity and efficiency. A highlight of this method is that one equivalent of each coupling partner is utilized. Building on these findings, a nonenzymatic, catalytic method for coupling tyrosine was also developed.