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431-90-3

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431-90-3 Usage

General Description

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

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

431-90-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,1,2,3,3-hexafluoro-3-iodopropane

1.2 Other means of identification

Product number -
Other names 1,1,1,2,3,3-hexafluoro-3-iodo-propane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:431-90-3 SDS

431-90-3Downstream Products

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.

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