69064-33-1 Usage
Uses
Used in Coatings Industry:
Perfluoroadamantane is used as a hydrophobic and lipophobic coating agent for creating water and oil repellent surfaces. Its application enhances the durability and resistance of materials against environmental elements, making it ideal for use in protective coatings.
Used in Material Manufacturing:
In the material manufacturing industry, perfluoroadamantane serves as a key component in the production of high-performance membranes and films. Its unique structure contributes to the development of materials with superior barrier properties and chemical resistance.
Used in Chemical Synthesis:
Perfluoroadamantane is utilized as a building block in the synthesis of other fluorinated compounds. Its chemical structure and properties make it a valuable precursor for creating complex molecules with specific applications in various fields, including pharmaceuticals and specialty chemicals.
Overall, perfluoroadamantane's versatility and unique properties position it as a valuable compound in a range of industrial and research applications, from enhancing material performance to contributing to the development of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 69064-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,6 and 4 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69064-33:
(7*6)+(6*9)+(5*0)+(4*6)+(3*4)+(2*3)+(1*3)=141
141 % 10 = 1
So 69064-33-1 is a valid CAS Registry Number.
InChI:InChI=1/C10F16/c11-1-5(15,16)2(12)8(21,22)3(13,6(1,17)18)10(25,26)4(14,7(1,19)20)9(2,23)24
69064-33-1Relevant academic research and scientific papers
Molecular structure of perfluoroadamantane from gas-phase electron diffraction
Hargittai, Istvan,Brunvoll, Jon,Sonoda, Takaaki,Takashi, Abe,Baba, Hajime
, p. 55 - 58 (2007/10/03)
The following bond lengths (r(g)) and bond angles have been determined for perfluomadamantane from gas-phase electron diffraction: C-C 1.560 ± 0.003, C(F2)-F 1.340 ± 0.005, C(F)-F 1.363 ± 0.010 A, CC(F2)C 107.7 ± 0.9, CC(F)C 110.3 ± 0.4, FC(F2)F 106.9 ± 0.4, C(F2)CF 108.6 ± 0.4 and C(F)CF 110.5 ± 0.2°. Perfluorination is found to expand the adamantane cage, characterized by a 0.02 A lengthening of the C-C bonds.
