50561-93-8 Usage
Uses
Used in Organic Synthesis:
(2-fluoroethyl)benzene is utilized as a starting material for the synthesis of a wide range of organic compounds, contributing to the development of new chemical entities and products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2-fluoroethyl)benzene serves as a key intermediate in the production of various drugs, playing a crucial role in advancing medical treatments and therapies.
Used in Agrochemical Manufacturing:
(2-fluoroethyl)benzene is employed as a component in the manufacturing of agrochemicals, which are essential for enhancing crop protection and agricultural productivity.
Used in Dye and Pigment Production:
This chemical compound is also used in the creation of dyes and pigments, which are vital for coloring textiles, plastics, and other materials in various industries.
Used as a Solvent:
(2-fluoroethyl)benzene is applied as a solvent in numerous industrial processes, facilitating chemical reactions and aiding in the manufacturing of different products.
Safety Note:
Due to its flammable nature and potential to cause irritation to the skin, eyes, and respiratory system at high concentrations, (2-fluoroethyl)benzene should be handled with caution.
Check Digit Verification of cas no
The CAS Registry Mumber 50561-93-8 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 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 50561-93:
(7*5)+(6*0)+(5*5)+(4*6)+(3*1)+(2*9)+(1*3)=108
108 % 10 = 8
So 50561-93-8 is a valid CAS Registry Number.
50561-93-8Relevant 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.
