22819-47-2 Usage
Uses
Used in Electronics Industry:
CIS-1,1,2,2,3,4-HEXAFLUOROCYCLOBUTANE is used as a refrigerant and insulating gas in the electronics industry, leveraging its stable and non-reactive nature to maintain the performance and longevity of electronic components.
Used in Production of Insulating Foams:
In the manufacturing sector, CIS-1,1,2,2,3,4-HEXAFLUOROCYCLOBUTANE serves as a blowing agent in the production of insulating foams, contributing to the creation of efficient thermal insulation materials.
Used in Precision Cleaning Applications:
CIS-1,1,2,2,3,4-HEXAFLUOROCYCLOBUTANE is utilized as a component in precision cleaning solvents and equipment, capitalizing on its ability to remove contaminants without damaging sensitive materials or components.
Used in Manufacturing Industry:
CIS-1,1,2,2,3,4-HEXAFLUOROCYCLOBUTANE is used as a component in the manufacture of various industrial products, taking advantage of its chemical properties to enhance the performance and quality of the final products.
It is crucial to handle CIS-1,1,2,2,3,4-HEXAFLUOROCYCLOBUTANE with care and adhere to safety regulations to mitigate any potential environmental impact and health hazards associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 22819-47-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,8,1 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22819-47:
(7*2)+(6*2)+(5*8)+(4*1)+(3*9)+(2*4)+(1*7)=112
112 % 10 = 2
So 22819-47-2 is a valid CAS Registry Number.
InChI:InChI=1/C4H2F6/c5-1-2(6)4(9,10)3(1,7)8/h1-2H/t1-,2+
22819-47-2Relevant academic research and scientific papers
Fluorination of fluoro-cyclobutene with high-valency metal fluoride
Mizukado, Junji,Matsukawa, Yasuhisa,Quan, Heng-Dao,Tamura, Masanori,Sekiya, Akira
, p. 79 - 84 (2007/10/03)
Fluorinations of 1,4,4-trifluorocyclobutene and 3,3,4,4- tetrafluorocyclobutene using high-valency metal fluorides such as CoF 3, MnF3, AgF2, CeF4 and KCoF 4, and elemental fluorine were examined. In these reactions with CoF3 and MnF3, vic-difluorination proceeded mainly. While, 1,4,4-trifluorocyclobutene yielded 3,3,4,4-tetrafluorocyclobutene, and 3,3,4,4-tetrafluorocyclobutene yielded 1,3,3,4,4-pentafluorocyclobutene mainly in the case of AgF2. The further fluorinated products were increased under severer conditions. Also, the plausible reaction mechanism was suggested.
Reductive dehalogenation of polyhalofluorocarbons with tributyltin hydride
Puy, Michael Van Der,Belter, Randolph K.,Borowski, Ralph J.,Ellis, Lois A. S.,Persichini, Phillip J.,et al.
, p. 59 - 64 (2007/10/02)
The reduction of polyhalofluorocarbons, including ClCF2CFClCF2Cl, (ClCF2CFCl)2, ICH2(CF2)3CH2I and vicinal dichloroperfluorocycloalkanes, with tributyltin hydride gave the corresponding hydrofluorocarbons in good to excellent yield.The results are compared with similar reductions with other reducing agents, and to tin hydride reductions of non-fluorinated analogs. - Keywords: Reductive dehalogenation; Polyfluorocarbons; Tributyltin hydride; NMR spectroscopy; Hydrofluorocarbons
