20825-07-4

Usage

Uses

Used in Chemical Industry:
1,1,1,5,5,6,6,6-OCTAFLUORO-2,4-HEXANEDIONE is used as an extraction agent for the removal of transition metal ions from water into fluorous solvents. This application is valuable for purifying water samples and preventing contamination in various chemical processes.
Used in Electronics Industry:
1,1,1,5,5,6,6,6-OCTAFLUORO-2,4-HEXANEDIONE is used as a chelating agent in the chemical vapor deposition (CVD) process for the production of barium fluoride thin films. Barium fluoride thin films are essential components in various electronic devices, such as optical components, sensors, and solar cells, due to their unique optical and electrical properties. The use of 1,1,1,5,5,6,6,6-OCTAFLUORO-2,4-HEXANEDIONE in this process ensures the formation of high-quality thin films with desired properties.

InChI:InChI=1/C6H2F8O2/c7-4(8,6(12,13)14)2(15)1-3(16)5(9,10)11/h1H2

Upstream product

• 23405-28-9 3,3-dihydroperfluorohexane-2,2,4,4-tetraol 
• 421-50-1 1,1,1-trifluoro-2-propanone 
• 426-65-3 ethyl Pentafluoropropionate 
• 378-75-6 perfluoropropionic acid methyl ester 

Downstream Products

• 866638-90-6 2-(3-methyl-4-nitro-phenyl)-5-pentafluoroethyl-3-trifluoromethyl-3,4-dihydro-2H-pyrazol-3-ol 

Relevant academic research and scientific papers

Synthesis, NMR, photoluminescence studies and intramolecular energy transfer process of europium(III) complexes

The studies related to the synthesis and luminescence properties of five europium(III) complexes of the type [Eu(OFHD)L] where OFHD is deprotonated 1,1,1,5,5,6,6,6-octafluorohexane-2,4-dione and L is H2O (C1), 2,2′-biquinoline (C2), neocuproine

New efficient synthetic routes to trifluoromethyl substituted pyrazoles and corresponding β-diketones

An improved and more efficient synthesis procedure for trifluoromethyl substituted pyrazoles, namely 3,5-bis(trifluoromethyl)-1H-pyrazole (1a), 5-(pentafluoroethyl)-3-(trifluoromethyl)-1H-pyrazole (1b), 5-(heptafluoropropyl)-3-(trifluoromethyl)-1H-pyrazol

Reaction of 3H-perfluoroalk-2-enes with ammonia

3H-Perfluoroalk-2-enes react with aqueous ammonia to form polyfluorinated iminoenamines, from which hexafluoroacetylacetone and its analogs were synthesized.