66804-94-2 Usage
Molecular structure
The chemical has a complex molecular structure with multiple fluorine-containing functional groups, including difluoro, pentafluoroethoxy, tetrafluoroethoxy, and heptafluoropropane.
Fluorination level
The compound has a high level of fluorination, which can contribute to its stability and potentially affect its reactivity and solubility properties.
Stability
Due to its high fluorination level, the compound is likely to be stable.
Reactivity
The high fluorination level may affect the reactivity of the compound.
Solubility
The high fluorination level may also affect the solubility properties of the compound.
Industrial applications
The compound may have potential industrial applications, particularly in areas such as pharmaceuticals, agrochemicals, and materials science.
Fluorinated nature
The compound is a fluorinated compound, which can contribute to its unique properties.
Functional groups
The compound contains various fluorine-containing functional groups, which can contribute to its unique properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 66804-94-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,0 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66804-94:
(7*6)+(6*6)+(5*8)+(4*0)+(3*4)+(2*9)+(1*4)=152
152 % 10 = 2
So 66804-94-2 is a valid CAS Registry Number.
66804-94-2Relevant articles and documents
PHOTOCHEMICAL FLUORINATION OF PERFLUOROPOLYETHER FUNCTIONAL DERIVATIVES
Marchionni, G.,Staccione, A.,Gregorio, G.
, p. 515 - 525 (1990)
Oligomeric perfluorinated polyethers bearing various carbonylic end groups are reacted, at low or moderate temperatures, with fluorine under the influence of UV light.Carboxylic acylfluoride, and trifluoromethylketone groups are quantitatively cleaved under these conditions, while fluoroformate groups are mainly transformed into stable fluoroxy derivatives.Some mechanistic aspects of these photoreactions are discussed.
