431-90-3 Usage
Uses
Used in Chemical Synthesis:
1,1,2,3,3,3-HEXAFLUOROPROPYL IODIDE is used as an intermediate in the synthesis of other organic compounds, contributing to the production of various chemical products.
Used in Fluorinated Material Production:
1,1,2,3,3,3-HEXAFLUOROPROPYL IODIDE is used as a key component in the production of fluorinated materials, which have a wide range of applications due to their unique properties.
Used in Pharmaceutical Industry:
1,1,2,3,3,3-HEXAFLUOROPROPYL IODIDE is used as a reagent in the pharmaceutical industry, particularly in the synthesis of complex organic compounds that have potential medicinal applications.
Used in Organic Chemistry Research:
1,1,2,3,3,3-HEXAFLUOROPROPYL IODIDE is utilized as a reagent in organic chemistry research, aiding in the development and understanding of complex organic compounds and their reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 431-90-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,3 and 1 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 431-90:
(5*4)+(4*3)+(3*1)+(2*9)+(1*0)=53
53 % 10 = 3
So 431-90-3 is a valid CAS Registry Number.
InChI:InChI=1/C3HF6I/c4-1(2(5,6)7)3(8,9)10/h1H
431-90-3Relevant academic research and scientific papers
Free-radical Addition to Olefins. Part 26.-Kinetics of the Addition of Trifluoromethyl Radicals to Acetylene and Substituted Acetylenes
Soueni, Amr El,Tedder, John M.,Walton, John C.
, p. 89 - 100 (2007/10/02)
Absolute Arrhenius parameters have been determined for the addition of trifluoromethyl radicals to acetylene, propyne, but-2-yne, 1,1,1-trifluoropropyne and hexafluorobut-2-yne by a competitive method using the previously determined Arrhenius parameters for the addition of trifluoromethyl radicals to ethylene as standard. . Both the activation energies and the A-factors are larger than those for the addition of trifluoromethyl radicals to similarly substituted olefins.As a result of these opposing effects the rates of addition are similar.
