2729-28-4

Usage

Uses

Used in Electronics Industry:
1,1-dichloro-1,2,2,3,3,3-hexafluoropropane is used as a solvent in the electronics industry for its ability to dissolve various materials and facilitate manufacturing processes. However, due to its adverse environmental effects, it is being replaced by more environmentally friendly alternatives.
Used in Chemical Research:
In the field of chemical research, 1,1-dichloro-1,2,2,3,3,3-hexafluoropropane may be used as a reference compound or in the synthesis of other compounds. Its unique properties and reactivity can provide insights into the behavior of similar halogenated hydrocarbons.

InChI:InChI=1/C3Cl2F6/c4-2(5,8)1(6,7)3(9,10)11

Upstream product

• 422-87-7 1-chloro-1,2,2,3,3,3-hexafluoro-1-iodo-propane 
• 7782-50-5 chlorine 
• 116-14-3 polytetrafluoroethylene 
• 75-71-8 Dichlorodifluoromethane 
• 22736-17-0 hexafluorodiazopropane 
• 75-69-4 trichlorofluoromethane 
• 677-56-5 1,1,1,2,2,3-hexafluoropropane 

Downstream Products

• 354-34-7 trifluoroacetyl fluoride 
• 422-61-7 perfluoropropanoyl fluoride 

Relevant academic research and scientific papers

PROCESSES FOR THE SYNTHESIS OF 3-CHLOROPERFLUORO-2-PENTENE, OCTAFLUORO-2-PENTYNE, AND 1,1,1,4,4,5,5,5-OCTAFLUORO-2-PENTENE

Disclosed is a process comprising reacting CF3CF2CCI2CF2CF3 (CFC-41 -10mca) with hydrogen in the presence of a dehalogenation catalyst to produce CF3CF2CCI=CFCF3 (CFC-1419myx). Also disclosed herein is a process comprising reacting CF3CF2CCI=CFCF3 (CFC- 1419myx) with hydrogen in the presence of a dehalogenation catalyst to produce CF3CF2C≡CCF3 (octafluoro-2-pentyne). Also disclosed herein is a process comprising reacting CF3CF2CCI2CF2CF3 (CFC-41 -10mca) with hydrogen in the presence of a dehalogenation catalyst to produce CF3CF2C≡CCF3 (octafluoro-2-pentyne). In addition, a process for reacting CF3CF2C≡CCF3, in a pressure vessel, with a Lindlar catalyst and hydrogen to produce CF3CF2CH=CHCF3 (1,1,1,4,4,5,5,5-octafluoro-2- pentene) is disclosed.

19F nuclear magnetic resonance studies of halogenated propanes

The relationship between 19F chemical shifts in halogenated propanes and their structures are elucidated using MNDO calculations to determine the population of rotamers.The pairs of atom gauche to a fluorine atom and van der Waals interaction between the two terminal substituents are responsible for the 19F chemical shifts.The differences among chemical shifts in diastereomers are also discussed in terms of the conformation of molecule.