53392-78-2

Usage

Physical state

Colorless, flammable gas

Uses

a. Refrigerant
b. Precursor in the production of other fluorinated compounds

Industrial applications

Used as a solvent

Boiling point

Low (not specified in the material)

Odor

Odorless

Reactivity

Highly reactive

Safety hazards

a. Fire and explosion hazard if not handled properly
b. Potential environmental hazard

Disposal

Should be properly managed and disposed of to prevent harmful effects on the environment

Upstream product

• 592-41-6 1-hexene 
• 76-05-1 trifluoroacetic acid 
• 2314-97-8 iodotrifluoromethane 
• 693-02-7 hex-1-yne 
• 75-63-8 Bromotrifluoromethane 

Relevant academic research and scientific papers

Ultrasound-Promoted Selective Perfluoroalkylation on the Desired Position of Organic Molecules

Perfluoroalkylzinc iodides or bromides wich were prepared from perfluoroalkyl iodides or bromides and zinc powder in N,N-dimethylformamide or tetrahydrofuran with ultrasonic irradiation were found to behave as potential perfluoroalkylating reagents for the preparation of a wide variety of perfluoroalkylated compounds.Especially, the ultrasound-promoted asymmetric induction with perfluoroalkyl group on the asymmetrical carbon was achieved by the reaction of perfluoroalkyl halides with optically active enamines in the presence of zinc powder and a catalytic amount of dichlorobis(?-cyclopentadienyl)titanium.

ULTRASOUND-PROMOTED HYDRPERFLUOROALKYLATION OF ALKYNES WITH PERFLUOROALKYLZINC IODIDE AND COPPER(I) IODIDE

The reaction of perfluoroalkyl iodides with terminal alkynes and ultrasonically dispersed zinc in the presence of copper(I) iodide proceeded smoothly to give the corresponding vinyl perfluoroalkylides in good yields.