86692-88-8 Usage
Uses
Used in Pharmaceutical Applications:
[1,1-Biphenyl]-2,4-diol,2,4,6,6-tetramethyl-(9CI) is used as an intermediate compound for the synthesis of various pharmaceutical products due to its unique chemical structure and properties.
Used in Agrochemical Applications:
In the agrochemical industry, [1,1-Biphenyl]-2,4-diol,2,4,6,6-tetramethyl-(9CI) is used as a building block for the development of new agrochemicals, potentially enhancing their effectiveness and targeting specific pests or diseases.
Used in Organic Synthesis:
As a derivative of biphenyl, [1,1-Biphenyl]-2,4-diol,2,4,6,6-tetramethyl-(9CI) is used as a key building block in the synthesis of other organic compounds, contributing to the development of novel materials and chemicals.
Used in Antioxidant Applications:
Given its potential antioxidant properties, [1,1-Biphenyl]-2,4-diol,2,4,6,6-tetramethyl-(9CI) may be used as an additive in the food and cosmetic industries to extend shelf life and protect against oxidative damage.
Used in Antibacterial Applications:
[1,1-Biphenyl]-2,4-diol,2,4,6,6-tetramethyl-(9CI)'s potential antibacterial properties make it a candidate for use in the development of new antimicrobial agents, particularly in the medical and hygiene product sectors.
Check Digit Verification of cas no
The CAS Registry Mumber 86692-88-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,9 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 86692-88:
(7*8)+(6*6)+(5*6)+(4*9)+(3*2)+(2*8)+(1*8)=188
188 % 10 = 8
So 86692-88-8 is a valid CAS Registry Number.
86692-88-8Relevant academic research and scientific papers
Oxidativ Coupling of Phenols. Part 6. A Study of the Role of Spin Density Factors on the Product Composition in the Oxidations of 3,5-Dimethylphenol and Phenol
Armstrong, David R.,Cameron, Colin,Nonhebel, Derek C.,Perkins, Peter G.
, p. 563 - 568 (2007/10/02)
Oxidations of both 3,5-dimethyphenol and phenol with di-t-butyl peroxide at 140 degC gave as the major product the ortho-ortho-C-C coupled dimer, while oxidations with di-t-butyl peroxyoxalate at room temperature give much more of the ortho-para-C-C dimer.The results are not consistent either with the spin density distribution in the phenoxyl radical intermediates or with steric effects being the major factor which determines the product composition.It is proposed that the two phenoxyl radicals involved in coupling preferentially approach each other in a 'sandwich like' manner with the oxigens in a 1,3-relationship.
THE ROLE OF STEREOELECTRONIC FACTORS IN THE OXIDATION OF PHENOLS
Armstrong, David R.,Breckenridge, Robin J.,Cameron, Colin,Nonhebel, Derek C.,Pauson, Peter L.,Perkins, Peter G.
, p. 1071 - 1074 (2007/10/02)
The oxidative coupling of both 3,5-dimethylphenol and phenol leads to the ortho-ortho and ortho-para coupled products as the predominant C-C dimers: stereoelectronic factors determine the preferred mode of approach of the phenoxyl radicals.
