392-61-0 Usage
Uses
Used in Chemical Synthesis:
2,4-difluoro-1,3,5-trimethylbenzene is used as a precursor in the production of other chemicals, playing a crucial role in the synthesis of a range of compounds for different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,4-difluoro-1,3,5-trimethylbenzene is utilized as a starting material or intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines.
Used in Solvent Applications:
2,4-difluoro-1,3,5-trimethylbenzene serves as a solvent in a variety of industrial processes, where its ability to dissolve other substances makes it a valuable component in the manufacturing of products.
Used in Coatings and Adhesives Manufacturing:
2,4-difluoro-1,3,5-trimethylbenzene is employed in the production of coatings and adhesives, where its properties enhance the performance and characteristics of these materials.
Safety Precautions:
It is important to handle 2,4-difluoro-1,3,5-trimethylbenzene with care, as it can be harmful if inhaled, ingested, or comes into contact with the skin. Adequate safety measures should be implemented during its use to ensure the well-being of individuals working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 392-61-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 392-61:
(5*3)+(4*9)+(3*2)+(2*6)+(1*1)=70
70 % 10 = 0
So 392-61-0 is a valid CAS Registry Number.
392-61-0Relevant academic research and scientific papers
Fluorination of aromatic compounds with N-fluorobenzenesulfonimide under solvent-free conditions
Andreev,Borodkin,Shubin
scheme or table, p. 1468 - 1473 (2010/03/24)
Reactions of N-fluorobenzenesulfonimide with methylbenzenes, phenols, and phenol ethers were studied under solvent-free conditions. The rate constant ratio for the reactions with mesitylene and durene indicates polar mechanism of the process. Solvent-free fluorination of aromatic compounds with N-fluorobenzenesulfonimide in some cases is more selective than reactions with other N-F reagents in a solvent.
Effect of Catalyst on the Fluorination of Methyl-Substituted Benzenes with Xenon Difluoride
Stavber, Stojan,Zupan, Marko
, p. 2223 - 2226 (2007/10/02)
The course of acid-catalyzed liquid-phase fluorination of methyl-substituted benzene derivatives with xenon difluoride depends strongly on the structure and concentration of the substrate, its molar ratio to xenon difuoride, and the catalyst.HF-catalyzed
