336-19-6

Usage

Uses

Used in Industrial Applications:
1,2-Dichlorooctafluorocyclohex-1-ene is used as a refrigerant and solvent due to its unique properties, including its non-flammability and stability. It is particularly valued in industries where these characteristics are crucial for safety and performance.
Used in Chemical Synthesis:
In the chemical industry, 1,2-Dichlorooctafluorocyclohex-1-ene may also serve as a precursor or intermediate in the synthesis of other fluorinated compounds, leveraging its high fluorine content for specific chemical reactions and product development.
Used in Environmentally Friendly Technologies:
Given its low toxicity and non-hazardous nature, 1,2-Dichlorooctafluorocyclohex-1-ene can be utilized in the development of environmentally friendly technologies, such as eco-friendly refrigerants and solvents, contributing to reduced environmental impact and improved sustainability in various sectors.

InChI:InChI=1/C6Cl2F8/c7-1-2(8)4(11,12)6(15,16)5(13,14)3(1,9)10

Upstream product

• 15145-21-8 1-chloro-2,3,3,4,4,5,5,6,6-nonafluorocyclohexene 
• 118-74-1 hexachlorobenzene 

Downstream Products

• 4545-93-1 3,3,4,4,5,5,6,6-Octafluor-cyclohex-1-en-1,2-diphosphonsaeure-1,2-tetraaethylester 
• 859-96-1 Octafluor-1,2-bis-phenylmercapto-cyclohexen 
• 336-08-3 perfluoroadipic acid 
• 1449075-14-2 C₁₈H₁₆F₈N₂S₂ 
• 1449075-18-6 C₂₀H₁₂Br₂F₈O₄S₂ 
• 1449075-17-5 C₁₈H₈Cl₂F₈O₂S₂ 
• 1449075-16-4 C₂₀H₁₄F₈O₂S₂ 
• 1449075-15-3 C₂₄H₁₄F₈S₂ 
• 24512-34-3 1-lithium 2-chloro perfluoro cyclohexene 
• 24480-71-5 (2-Chlor-decafluor-cyclohexyl)-methyl-ether 
• 76170-40-6 2-chloro-3,3,4,4,5,5,6,6-octafluoro-1-cyclohexene-1-thiol 

Relevant academic research and scientific papers

Method for synthesizing high-purity hexafluoro-1, 3-butadiene

The invention relates to a method for synthesizing high-purity hexafluoro-1, 3-butadiene, and belongs to the field of organic chemical synthesis. The method for synthesizing the hexafluoro-1, 3-butadieneI is characterized by comprising: heating hexachlorobenzene, chlorine and anhydrous hydrogen fluoride under the action of a catalyst to generate 1, 2-dichloro-3, 3, 4, 4, 5, 5, 6, 6-octafluorocyclohexene; heating the 1, 2-dichloro-3, 3, 4, 4, 5, 5, 6, 6-octafluorocyclohexene and a solvent under the action of a strong oxidant to generate 1, 6-octafluoroadipic acid; and finally, heating the 1, 6-octafluoroadipic acid and a solvent under the action of sodium hydroxide to generate sodium fluoride, water, carbon dioxide and hexafluoro-1, 3-butadiene, performing water removal and carbon dioxide removal treatment on the mixed gas to obtain the high-purity hexafluoro-1, 3-butadiene. The raw materials are cheap and convenient to obtain; the catalyst has good stability and long service life; theproduct separation and purification are simple; and industrial production is easy.

REACTION OF POLYFLUORINATED CYCLOALKANES WITH VANADIUM, ANTIMONY, AND NIOBIUM PENTAFLUORIDES

Polyfluorinated cycloalkanes are fluorinated by vanadium pentafluoride at 25-60 deg C.Conjugation between the C=C bond of the cycloalkene and the aromatic ring facilitates the reaction, whereas the reactivity of the unconjugated olefin fragment is lower than or is equal to that of the aromatic ring.The antimony pentafluoride fluorinates polyhalogenocyclohexenes at 150 deg C, while niobium pentafluoride does not exhibit fluorinating characteristics under these conditions.