4526-39-0 Usage
Uses
Used in Polymers and Plastics Industry:
2,6-BIS(METHYLTHIOMETHYL)-4-METHYLPHENOL is used as an antioxidant and UV stabilizer for polymers and plastics to extend their durability and protect them from environmental factors such as sunlight and heat.
Used in Rubber Industry:
In the rubber industry, 2,6-BIS(METHYLTHIOMETHYL)-4-METHYLPHENOL serves as an essential additive to enhance the resistance of rubber products to degradation, thereby improving their longevity and performance.
Used in Adhesives and Sealants:
2,6-BIS(METHYLTHIOMETHYL)-4-METHYLPHENOL is used as a stabilizing agent in the production of adhesives and sealants to improve their resistance to environmental factors and increase their overall durability.
Used in Coatings:
2,6-BIS(METHYLTIOMETHYL)-4-METHYLPHENOL is also utilized in the formulation of coatings to provide protection against UV radiation and oxidative stress, ensuring the coated surfaces maintain their integrity and appearance over time.
Used in Health and Wellness Research:
2,6-BIS(METHYLTHIOMETHYL)-4-METHYLPHENOL has been studied for its potential health benefits, including its antioxidant and anti-inflammatory properties, indicating possible applications in the development of health supplements or pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 4526-39-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4526-39:
(6*4)+(5*5)+(4*2)+(3*6)+(2*3)+(1*9)=90
90 % 10 = 0
So 4526-39-0 is a valid CAS Registry Number.
4526-39-0Relevant academic research and scientific papers
Selective ortho-Methylthiomethylation of Phenols with Dimethyl Sulphoxide and Thionyl Chloride
Sato, Kikumasa,Inoue, Seiichi,Ozawa, Kimio,Tazaki, Michiko
, p. 2715 - 2719 (2007/10/02)
Thionyl chloride and phenyl chlorosulphinate have been shown to be useful activators for dimethyl sulphoxide in the selective preparation of ortho-methylthiomethylphenol via a sigmatropic rearrangement.By this process, ortho-methylthiomethylated phenols having a variety of 2- or 4-substituents (Me, Cl, OMe, NO2, and CO2Me) have been prepared in good yields.In contrast, similar reactions of 3-substituted phenols were affected by the electronic characters of the substituents.With more electron-donating groups such as OH and OMe in the 3-position, none of the expected products were obtained, but in the case of other 3-substituted phenols, two possible rearrangement products were obtained in moderate yields.
