60308-67-0 Usage
General Description
2-[1,1,2,3,3,3-Hexafluoro-2-(heptafluoropropoxy)propoxy]-2,3,3,3-tetrafluoropropanamide is a synthetic compound with a complex chemical structure composed of fluorine, carbon, oxygen, and nitrogen atoms. It belongs to the class of perfluorinated compounds, which are known for their high stability and resistance to chemical and thermal degradation. This specific chemical is used in various industrial applications such as in the production of fluorinated polymers, surfactants, and lubricants, as well as in electronics manufacturing. However, due to its fluorochemical nature, it has raised concerns about its potential impact on human health and the environment, particularly in relation to its persistence in the environment and potential toxicity. Therefore, the use and regulation of this compound are subject to ongoing scrutiny and research.
Check Digit Verification of cas no
The CAS Registry Mumber 60308-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,3,0 and 8 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60308-67:
(7*6)+(6*0)+(5*3)+(4*0)+(3*8)+(2*6)+(1*7)=100
100 % 10 = 0
So 60308-67-0 is a valid CAS Registry Number.
60308-67-0Relevant articles and documents
SYNTHESES AND DEGRADATIONS OF FLUORINATED HETEROCYCLICS. IV. IMIDOYLAMIDOXIMES, 1,2,4-OXADIAZOLE PRECURSORS
Paciorek, K. J. L.,Ito, T. I.,Nakahara, J. H.,Kaufman, J.,Kratzer, R. H.,Rosser, R. W.
, p. 51 - 62 (2007/10/02)
Perfluoroalkylether amidoximes free from amide-contamination were prepared from imidate esters.The amidoximes were stable at 110 deg C; at ca. 170 deg C partial decomposition to 1,2,4-oxadiazoles, admixed with other compounds, took place.Interactions between nitriles and amidoximes at 50 deg C resulted in the formation of imidoylamidoximes; these dissociated readily into their constituents when subjected to higher temperatures.At 70 deg C and above, in the presence of excess nitrile or other ammonia acceptors, the imidoylamidoximes afforded high yields of the corresponding 1,2,4-oxadiazoles.
