1198-61-4

Usage

Uses

Used in Chemical Production:
1,3-Dichlorotetrafluorobenzene is utilized as a key component in the synthesis of other chemicals, contributing to the diversity of chemical products available for different industries.
Used as an Industrial Solvent:
In various industrial processes, 1,3-Dichlorotetrafluorobenzene is employed as a solvent, leveraging its properties to dissolve and process materials effectively.
Used in Organic Synthesis:
1,3-Dichlorotetrafluorobenzene serves as a reagent in organic synthesis reactions, playing a crucial role in the formation of complex organic molecules.
Environmental and Health Considerations:
1,3-Dichlorotetrafluorobenzene is recognized as hazardous to human health and the environment. It is toxic if ingested, inhaled, or absorbed through the skin, and it can persist in the environment, leading to bioaccumulation in organisms. Therefore, its use requires careful handling and proper disposal to mitigate potential negative impacts on both human health and the environment.

InChI:InChI=1/C6Cl2F4/c7-1-3(9)2(8)5(11)6(12)4(1)10

Upstream product

• 392-56-3 Hexafluorobenzene 
• 118-74-1 hexachlorobenzene 
• 319-88-0 1,3,5-trichlorotrifluorobenzene 

Downstream Products

• 27602-32-0 m-chlorotetrafluorotrimethylsilylbenzene 
• 13332-11-1 1-Chlor-4-methoxy-2,3,6-trifluorbenzol 
• 13555-12-9 1-Chlor-2-methoxy-3,4,6-trifluorbenzol 
• 13332-02-0 1-Chlor-4-dimethylamino-2.3.6-trifluor-benzol 
• 13332-01-9 1-Chlor-2-dimethylamino-3.4.6-trifluor-benzol 
• 19998-03-9 2,4-dichlorotrifluorophenylhydrazine 
• 2280-52-6 2,4-bis(trifluoromethyl)-trifluorophenylhydrazine 
• 4125-57-9 2,4-dichloro-3,5,6-trifluoroaniline 
• 5172-06-5 1-chloro-2,3,4,6-tetrafluorobenzene 
• 20174-07-6 2,4-dichlorotetrafluoroanisole 

Relevant academic research and scientific papers

Chloro- and bromo-defluorination of hexafluorobenzene and octafluorotoluene

Halo(chloro, bromo)defluorination of perfluorobenzaene and toluene efficiently occurs under the action of appropriate alkali metal halides in the presence of hexaethylguanidinium chloride in catalytic amount. The relative efficiency of halide anions and m

Synergism in catalytic halogen-exchange fluorination of 4-chloronitro- and dichlorotetrafluorobenzenes

Synergism was studied in catalytic halogen-exchange fluorination of 4-chloronitro- and dichlorotetrafluorobenzenes. The synergistic effect in the fluorination of chloroaromatic compounds with potassium fluoride was mainly attributed to separation of the activation functions of catalysts with respect to substrate molecules.

Catalytic and noncatalytic ammonolysis of polyfluorinated 1,3-dichlorobenzenes

Reactions of 1,3-dichlorotetrafluorobenzene and 1,3-dichloro-2,4,6-trifluorobenzene with aqueous ammonia in the presence and in the absence of copper(I) salt lead to fluorine replacement by amino group in the para and ortho positions with respect to the chlorine atom. Ammonolysis of the resulting chloropolyfluoroanilines in the absence of a catalyst involves replacement of fluorine atom in the meta position with respect to the amino group. In the presence of copper(I) salt, catalytic aminodechlorination occurs at the para and ortho positions with respect to the amino group introduced in the first stage.