83168-66-5 Usage
General Description
(E,Z)-(CF3CF=CF)2 is a chemical compound with the molecular formula C6F12. It is a perfluorinated compound, which means it contains only carbon and fluorine atoms. The compound exists in both the E and Z configurations, which refer to the positions of the fluorine atoms on the carbon-carbon double bond. It is a highly stable and non-reactive compound, making it useful for a variety of industrial applications. Its properties, such as high thermal and chemical stability, make it suitable for use in electronics, refrigeration, and as a fire extinguishing agent. Additionally, its low toxicity and non-flammability make it a desirable alternative to other chemical compounds in certain applications.
Check Digit Verification of cas no
The CAS Registry Mumber 83168-66-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,1,6 and 8 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 83168-66:
(7*8)+(6*3)+(5*1)+(4*6)+(3*8)+(2*6)+(1*6)=145
145 % 10 = 5
So 83168-66-5 is a valid CAS Registry Number.
InChI:InChI=1/C6F10/c7-1(3(9)5(11,12)13)2(8)4(10)6(14,15)16/b3-1-,4-2+
83168-66-5Relevant articles and documents
ISOMERIC TRANSFORMATIONS OF PERFLUORINATED DIENES BY THE ACTION OF ANTIMONY PENTAFLUORIDE
Petrov, V. A.,Belen'kii, G. G.,German, L. S.
, p. 333 - 339 (1989)
-
Kinetic and Thermodynamic Studies of the Thermal Electrocyclic Interconversions of Perfluorinated Dienes and Cyclobutenes
Dolbier, Jr., William R.,Koroniak, Henryk,Burton, Donald J.,Heinze, Pamela L.,Bailey, A.R.,et al.
, p. 219 - 225 (2007/10/02)
Detailed kinetic and thermodynamic analyses were carried out for the thermal interconversions of (Z,Z)- and (E,E)-perfluoro-2,4-hexadienes with trans-perfluoro-3,4-dimethylcyclobutene, (E,Z)-perfluoro-2,4-hexadiene with perfluoro-cis-3,4-dimethylcyclobutene, (Z,Z)- and (E,E)-perfluoro-3,5-octadienes with trans-perfluoro-3,4-diethylcyclobutene, and (Z)- and (E)-perfluoro-1,3-pentadiene with perfluoro-3-methylcyclobutene.In each case the (Z,Z)- or (Z)-dienes exhibited substantial kinetic advantage over the (E,E)-or (E)-dienes in their cyclization precesses.
