431-90-3 Usage
Description
1,1,2,3,3,3-HEXAFLUOROPROPYL IODIDE is a colorless liquid chemical compound with the molecular formula C3H2F6I. It is primarily used as an intermediate in the synthesis of other organic compounds and is known for its use in various industrial processes, particularly in the production of fluorinated materials and pharmaceuticals. 1,1,2,3,3,3-HEXAFLUOROPROPYL IODIDE is also used as a reagent in organic chemistry, particularly in the synthesis of complex organic compounds. However, it is considered a hazardous material and should be handled with caution due to its potential health and environmental risks.
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 articles and documents
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.
