6669-01-8 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(PENTAFLUOROPHENOXY)ETHYL BROMIDE is used as a building block for the synthesis of pharmaceuticals, as it can introduce the pentafluorophenyl group into drug molecules, enhancing their properties and effectiveness.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-(PENTAFLUOROPHENOXY)ETHYL BROMIDE is used as an intermediate for the development of new agrochemicals, where the pentafluorophenyl group can improve the performance and selectivity of these compounds.
Used in Organic Synthesis:
2-(PENTAFLUOROPHENOXY)ETHYL BROMIDE is used as a versatile reagent in organic synthesis, allowing chemists to incorporate the pentafluorophenyl group into a wide range of organic molecules for various applications.
Used in the Synthesis of Fluorinated Compounds:
As a precursor for the synthesis of fluorinated compounds, 2-(PENTAFLUOROPHENOXY)ETHYL BROMIDE is utilized to create molecules with unique properties, such as enhanced stability and reactivity, which are valuable in various chemical and material applications.
Used in Flame Retardant Development:
2-(PENTAFLUOROPHENOXY)ETHYL BROMIDE has been studied for its potential use as a flame retardant, where its chemical structure could contribute to improving the fire resistance of materials.
Used in Polymer Synthesis:
In the field of polymer chemistry, 2-(PENTAFLUOROPHENOXY)ETHYL BROMIDE is used as a reagent in the synthesis of polymers, where the introduction of the pentafluorophenyl group can modify the polymer's properties, such as thermal stability and chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 6669-01-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,6 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6669-01:
(6*6)+(5*6)+(4*6)+(3*9)+(2*0)+(1*1)=118
118 % 10 = 8
So 6669-01-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H4BrF5O/c9-1-2-15-8-6(13)4(11)3(10)5(12)7(8)14/h1-2H2
6669-01-8Relevant academic research and scientific papers
Inter- and Intramolecular Aryl–Aryl Interactions in Partially Fluorinated Ethylenedioxy-bridged Bisarenes**
Weddeling, Jan-Henrik,Vishnevskiy, Yury V.,Neumann, Beate,Stammler, Hans-Georg,Mitzel, Norbert W.
supporting information, p. 16111 - 16121 (2020/10/28)
Several ethylenedioxy-bridged bisarenes with a variety of type and number of aryl groups were synthesized to study non-covalent dispersion-driven inter- and intramolecular aryl–aryl interactions in the solid state and gas phase. Intramolecular interactions are preferably found in the gas phase. DFT calculations with and without dispersion correction show larger interacting aromatic groups increase the stabilization energy of folded conformers and decrease the intermolecular centroid–centroid distance. Single-molecule structures generally adopt folded conformations with short intramolecular aryl–aryl contacts. Gas electron diffraction experiments were performed exemplarily for 1-(pentafluorophenoxy)-2-(phenoxy)ethane. A new procedure for structure refinement was developed to deal with the conformational complexity of such molecules. The results are an experimental confirmation of the existence of folded conformations of this molecule with short intramolecular aryl–aryl distances in the gas phase. Solid-state structures are dominated by stretched structures without intramolecular aryl–aryl interactions but interactions with neighboring molecules.
INHIBITORS OF ANTHRAX LETHAL FACTOR
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Page/Page column 55, (2008/06/13)
Methods, compounds and compositions for preventing and treating anthrax infections by inhibiting Anthrax Lethal Factor (LF) activity.
