53692-47-0 Usage
Uses
Used in Industrial Applications:
1-Bromopentafluoropropene is used as a key intermediate in the synthesis of various fluorinated compounds for industrial purposes. Its unique properties, such as thermal stability and chemical resistance, make it a valuable component in the production of specialty materials and chemicals.
Used in Chemical Research:
1-Bromopentafluoropropene serves as a valuable research compound in the field of organofluorine chemistry. Its reactivity and structural characteristics allow scientists to explore new reaction pathways and develop novel synthetic methods, contributing to the advancement of chemical knowledge and technology.
Used in Material Science:
1-Bromopentafluoropropene is used as a building block in the development of new materials with enhanced properties, such as improved thermal stability, chemical resistance, and mechanical strength. Its incorporation into polymers and other materials can lead to the creation of innovative products with applications in various industries, including aerospace, automotive, and electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 53692-47-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,9 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53692-47:
(7*5)+(6*3)+(5*6)+(4*9)+(3*2)+(2*4)+(1*7)=140
140 % 10 = 0
So 53692-47-0 is a valid CAS Registry Number.
InChI:InChI=1/C3BrF5/c4-2(6)1(5)3(7,8)9/b2-1-
53692-47-0Relevant academic research and scientific papers
Electrophilic reactions of fluorocarbons under the action of aluminum chlorofluoride, a potent Lewis acid
Petrov, V. A.,Krespan, C. G.,Smart, B. E.
, p. 138 - 142 (2007/10/03)
A new Lewis acid - aluminum chlorofluoride - was demonstrated to be an effective catalyst for the isomerisation of fluoroolefins, polyfluorinated epoxides and cyclopropanes.At ambient temperature this catalyst converts perfluorobutadiene-1,3 into perfluorobutyne-2 and perfluoro(4-methylpentene-2) into perfluoro(2-methylpentene-2) in nearly quantitative yield.At 100 deg C, aluminum chlorofluoride causes the cleavage of perfluorinated tertiary amines. - Keywords: Electrophilic reactions; Fluorocarbons; Aluminum chlorofluoride; Lewis acid; NMR spectroscopy
