23012-94-4 Usage
General Description
Trans-1,1,2,2,3,4-Hexafluorocyclobutane is a type of perfluorocarbon compound. These are fully fluorinated organic compounds, also known as PFCs. PFCs are heat-resistant and do not readily react with other substances, making them incredibly durable and stable. PFCs also have unique characteristics such as being able to remain as a gas or a liquid over a wide range of temperature and pressure conditions. This means they can be used in a variety of applications, from cooling systems to fire extinguishers. However, due to their stability, PFCs can be harmful to the environment as they persist for a long time and have a high global warming potential. Trans-1,1,2,2,3,4-Hexafluorocyclobutane in particular is a cyclobutane derivative where all the hydrogen atoms have been replaced with fluorine. It is relatively uncommon, and not much is known about its specific properties or uses.
Check Digit Verification of cas no
The CAS Registry Mumber 23012-94-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,1 and 2 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 23012-94:
(7*2)+(6*3)+(5*0)+(4*1)+(3*2)+(2*9)+(1*4)=64
64 % 10 = 4
So 23012-94-4 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-/m1/s1
23012-94-4Relevant articles and documents
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.
