1559-86-0 Usage
Uses
Used in Pharmaceutical Industry:
1-bromo-2,3,4,6-tetrafluorobenzene serves as a crucial building block in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical sector, 1-bromo-2,3,4,6-tetrafluorobenzene is utilized for the synthesis of compounds that have applications in crop protection and pest control, contributing to enhanced agricultural productivity.
Used as a Solvent in Organic Synthesis:
1-bromo-2,3,4,6-tetrafluorobenzene also functions as a solvent in organic synthesis processes, facilitating various chemical reactions due to its properties as a liquid at room temperature.
Used as a Reagent in Polymer and Specialty Chemical Production:
Furthermore, it is employed as a reagent in the production of polymers and specialty chemicals, where its reactivity and stability play a significant role in the formation of desired end products.
Environmental Considerations:
Check Digit Verification of cas no
The CAS Registry Mumber 1559-86-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,5 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1559-86:
(6*1)+(5*5)+(4*5)+(3*9)+(2*8)+(1*6)=100
100 % 10 = 0
So 1559-86-0 is a valid CAS Registry Number.
InChI:InChI=1/C6HBrF4/c7-4-2(8)1-3(9)5(10)6(4)11/h1H
1559-86-0Relevant academic research and scientific papers
Method for producing tetrakis ( fluoroaryl) borate-magnesium compound
-
, (2008/06/13)
Fluoroaryl magnesium halide is reacted with a boron compound so that a molar ratio of the fluoroaryl magnesium halide to the boron compound is not less than 3.0 and not more than 3.7, so as to produce a tetrakis (fluoroaryl) borate·magnesium compound. With this method, there occurs no hydrogen fluoride which corrodes a producing apparatus and requires troublesome waste water treatment.
Reaction of polyfluoroaromatic compounds with electrophilic agents in the presence of tris(dialkylamino)phosphines: 7. * Replacement of a halogen by hydrogen in halogenopolyfluoroaromatic compounds
Bardin,Pressman
, p. 786 - 788 (2007/10/03)
A method was developed for the replacement of chlorine, bromine, and iodine in halopolyfluoroaromatic compounds by hydrogen under the action of P(NEt2)3 and a proton donor.
