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Perfluoro-2-iodo-3-methylbutane is a synthetic chemical compound with the molecular formula C5H3F13I. It is a halogenated hydrocarbon, characterized by the presence of 13 fluorine atoms, one iodine atom, and three hydrogen atoms. The compound features a 3-methylbutane backbone, with the iodine atom positioned at the 2nd carbon and the methyl group at the 3rd carbon. Due to its unique structure, perfluoro-2-iodo-3-methylbutane exhibits properties such as high chemical stability, low reactivity, and resistance to thermal degradation. These characteristics make it a potential candidate for various industrial applications, including the production of specialty polymers, surfactants, and as a precursor in the synthesis of other perfluorinated compounds. However, it is essential to consider the environmental and health implications associated with the use and disposal of such compounds, as some perfluorinated chemicals have been linked to adverse effects on human health and the environment.

7626-45-1

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7626-45-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7626-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,2 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7626-45:
(6*7)+(5*6)+(4*2)+(3*6)+(2*4)+(1*5)=111
111 % 10 = 1
So 7626-45-1 is a valid CAS Registry Number.

7626-45-1Downstream Products

7626-45-1Relevant academic research and scientific papers

Pyrolysis of branched-chain perfluoroalkanes in the presence of halogens

Tonelli, Claudio,Tortelli, Vito

, p. 125 - 128 (2007/10/03)

The thermal decomposition of some highly branched perfluoroalkanes in the presence of molecular halogens (Cl2, Br2, I2) has been studied.The clear-cut cleavage of the most hindered carbon-carbon bond and the trapping by halogens of the intermediate radicals so formed account for the product distribution.Kinetic measurements support a mechanism based on homolytic rupture of the perfluoroalkanes as the rate-determining step, followed by the fast reaction of the intermediates with halogens.

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