6390-59-6 Usage
General Description
"[1,1'-Biphenyl]-2,2'-diol, 3,3'-bis(1,1-dimethylethyl)-5,5'-dimethyl-" is a chemical compound with the molecular formula C26H34O2. It is a type of diol, meaning it contains two hydroxyl (OH) functional groups. [1,1'-Biphenyl]-2,2'-diol, 3,3'-bis(1,1-dimethylethyl)-5,5'-dimethyl- is also known as 3,3'-bis(tert-butyl)-5,5'-dimethyl-1,1'-biphenyl-2,2'-diol and is commonly used as an antioxidant and stabilizer in various industrial and consumer products. Its high stability and ability to prevent chemical degradation make it a valuable additive in plastics, rubbers, and other materials exposed to harsh environmental conditions. Additionally, this compound has also been studied for its potential pharmaceutical applications, particularly in the development of new drugs for the treatment of various medical conditions.
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.
