79348-71-3 Usage
Uses
Used in Pharmaceutical Industry:
2,4,6-Trifluorotoluene is used as a solvent in the synthesis of pharmaceuticals for its ability to dissolve a wide range of compounds, facilitating chemical reactions and improving the efficiency of drug production.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4,6-Trifluorotoluene serves as a solvent in the synthesis of agrochemicals, aiding in the production of effective and targeted pesticides and other agricultural chemicals.
Used in Dye Manufacturing:
2,4,6-Trifluorotoluene is utilized as a solvent in the manufacturing of dyes, contributing to the development of vibrant and stable colorants for various applications.
Used in Polymer Production:
2,4,6-Trifluorotoluene is used as an intermediate in the production of polymers, playing a crucial role in the synthesis of polymers with specific properties for use in plastics, coatings, and other materials.
Used in Coatings and Adhesives Formulation:
2,4,6-Trifluorotoluene is incorporated as a component in the formulation of certain coatings and adhesives, enhancing their performance characteristics such as adhesion strength and chemical resistance.
Used in Specialty Chemicals Production:
As an intermediate, 2,4,6-Trifluorotoluene is essential in the production of other specialty chemicals, broadening its applications across various industries.
Used in Refrigeration Applications:
Although not its primary use, 2,4,6-Trifluorotoluene has potential as a refrigerant in specific applications, offering an alternative to traditional refrigerants.
It is crucial to handle 2,4,6-Trifluorotoluene with care due to its potential to cause skin and eye irritation upon prolonged exposure to high concentrations, and respiratory issues from inhaling its vapors.
Check Digit Verification of cas no
The CAS Registry Mumber 79348-71-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,4 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79348-71:
(7*7)+(6*9)+(5*3)+(4*4)+(3*8)+(2*7)+(1*1)=173
173 % 10 = 3
So 79348-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F3/c1-4-6(9)2-5(8)3-7(4)10/h2-3H,1H3
79348-71-3Relevant academic research and scientific papers
REACTIONS OF AROMATIC COMPOUNDS WITH NUCLEOPHILIC REAGENTS IN LIQUID AMMONIA. REACTION OF POLYFLUORINATED DERIVATIVES OF BENZENE WITH SODIUM AMIDE
Shtark, A. A.,Chuikova, T. V.,Selivanova, G. A.,Shteingarts, V. D.
, p. 2271 - 2276 (2007/10/02)
Under the influence of sodium amide in liquid ammonia at a temperature no higher than -33 deg C pentafluorobenzene, 1,2,4,5-tetrafluorobenzene, and 1,3-difluorobenzene undergo deprotonation with the formation of fluorinated phenyl anions, which are resistant to the elimination of a fluoride ion and can be detected by the formation of the products from interaction with electrophiles (with the initial compound in the first case and with methyl iodide in the other two cases). 1,3,5-Trifluorobenzene behaves similarly in reaction with one equivalent of sodium amide, but with two equivalents of sodium amide this compound and 1,2,3,5-tetrafluorob enzene undergo substitution of a fluorine atom by an amino group with the formation of 3,5-di- and 3,4,5-trifluoroanilines respectively.This is clearly due to the double deprotonation of these compounds with the formation of polyfluorinated m-phenylene dianions, which are then converted with the elimination of a fluoride ion into the corresponding dehydrophenyl anions.
REACTION OF AROMATIC COMPOUNDS WITH NUCLEOPHILIC REAGENTS IN LIQUID AMMONIA IV.* THE NUCLEOPHILIC AND PROTOPHILIC ACTIVITY OF METHOXIDE AND HYDROXIDE IONS IN REACTIONS WITH POLYFLUORINATED AROMATIC COMPOUNDS
Shtark, A. A.,Chuikova, T. V.,Shteingarts, V. D.
, p. 960 - 967 (2007/10/02)
In the reaction of polyfluorinated derivatives of benzene with potassium methoxide in liquid ammonia a fluorine atom is substituted by a methoxy group.With potassium hydroxide reactions involving removal of a proton from a ring carbon atom take place preferentially.The possibility of polyfluoroarylation and methylation catalyzed by potassium hydroxide in polyfluorinated aromatic compounds, based on capture of the polyflurinated aryl anion by the electrophile, was demonstrated.
