50562-22-6 Usage
Uses
Used in Chemical Industry:
1-(2,2,2-trifluoroethyl)-3-(trifluoromethyl)benzene is used as a solvent in various industrial processes, taking advantage of its stability and solubility properties.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2,2,2-trifluoroethyl)-3-(trifluoromethyl)benzene serves as a reagent, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Production:
1-(2,2,2-trifluoroethyl)-3-(trifluoromethyl)benzene is utilized as a building block for the production of pharmaceuticals, where its unique structure and properties can be leveraged to create new medicinal compounds.
Used in Agrochemical Production:
Similarly, in the agrochemical industry, 1-(2,2,2-trifluoroethyl)-3-(trifluoromethyl)benzene is used as a precursor to develop new agrochemicals, potentially enhancing crop protection and yield.
It is crucial to handle 1-(2,2,2-trifluoroethyl)-3-(trifluoromethyl)benzene with care due to its potential harmful effects on health if mismanaged, emphasizing the need for proper safety measures during its use in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 50562-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,6 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 50562-22:
(7*5)+(6*0)+(5*5)+(4*6)+(3*2)+(2*2)+(1*2)=96
96 % 10 = 6
So 50562-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H6F6/c10-8(11,12)5-6-2-1-3-7(4-6)9(13,14)15/h1-4H,5H2
50562-22-6Relevant academic research and scientific papers
MECHANISMS OF FREE-RADICAL REACTIONS. XIII. MECHANISM AND SELECTIVITY OF THE FREE-RADICAL HALOGENATION OF ALKYL AROMATIC HYDROCARBONS WITH FLUOROALKYL SUBSTITUENTS
Dneprovskii, A. S.,Eliseenkov, E. V.,Mil'tsov, S. A.
, p. 317 - 324 (2007/10/02)
The free-radical chlorination and bromination of 1-fluoro-2-arylethanes and 1,1,1-trifluoro-2-arylethanes was studied by the method of competing reactions.In all cases a good correalation between log krel and the Brown ?+ constants was observed.The variation of the selectivity in the transition from one reaction series to the other indicates that two independent factors which determine the reactivity (the change in the dissociation energy of the C-H bond and the polar effect of the substituents) have a simultaneous effect.
