393-76-0 Usage
Uses
Used in Pharmaceutical Industry:
3,5-DINITRO-4-FLUOROBENZOTRIFLUORIDE is used as a synthetic intermediate for the development of various pharmaceuticals. Its unique chemical structure allows for the creation of new drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3,5-DINITRO-4-FLUOROBENZOTRIFLUORIDE is utilized as a precursor in the synthesis of pesticides and other crop protection agents, contributing to the development of more effective and targeted products.
Used in Dye and Pigment Manufacturing:
3,5-DINITRO-4-FLUOROBENZOTRIFLUORIDE is employed as a key component in the production of dyes and pigments, enabling the creation of a diverse array of colorants for various applications, including textiles, plastics, and printing inks.
Safety Precautions:
Given its highly reactive and toxic nature, 3,5-DINITRO-4-FLUOROBENZOTRIFLUORIDE requires careful handling and storage. It is essential to implement appropriate safety measures, such as using protective equipment, maintaining proper ventilation, and storing the compound away from reducing agents and ignition sources to prevent accidents and exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 393-76-0 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 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 393-76:
(5*3)+(4*9)+(3*3)+(2*7)+(1*6)=80
80 % 10 = 0
So 393-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H2F4N2O4/c8-6-4(12(14)15)1-3(7(9,10)11)2-5(6)13(16)17/h1-2H
393-76-0Relevant academic research and scientific papers
Clark, James H.,Tavener, Stewart J.
, p. 169 - 172 (1997)
The trifluoromethanethiolate anion may be generated in situ by the reaction of thiophosgene with potassium fluoride in acetonitrile. This system is used to prepare trifluoromethyl aryl sulfides from activated fluoro- and chloroaromatic substrates via nucleophilic substitution.
