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1071124-63-4

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1071124-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1071124-63-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,1,2 and 4 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1071124-63:
(9*1)+(8*0)+(7*7)+(6*1)+(5*1)+(4*2)+(3*4)+(2*6)+(1*3)=104
104 % 10 = 4
So 1071124-63-4 is a valid CAS Registry Number.

1071124-63-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (perfluoroethyl)(phenyl)-l<sup>3</sup>-iodanyl trifluoromethanesulfonate

1.2 Other means of identification

Product number -
Other names -

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:1071124-63-4 SDS

1071124-63-4Relevant articles and documents

Syntheses and properties of (perfluoroalkyl)phenyliodonium triflates (fits reagents) and their analogues

Umemoto, Teruo,Kuriu, Yuriko,Shuyama, Hideo,Miyano, Osamu,Nakayama, Shin-Ichi

, p. 37 - 56 (1986)

A variety of (per- and polyfluoroalkyl)phenyl- and p-fluorophenyliodonium triflates 3 were synthesized in good yields by the oxidation of the corresponding iodofluoroalkanes with trifluoroperacetic acid followed by the treatment with benzene or fluorobenzene and triflic acid. It was also shown that elemental fluorine was used as a substitute for the peracid. The use of fluorosulfonic, sulfuric, and methanesulfonic acids instead of triflic acid afforded the fluoroalkylaryliodonium fluorosulfonates 5, sulfates 6, and methanesulfonate 7, respectively. Similarly perfluoroalkylene-α,ω-bisaryliodonium triflates 10 were synthesized from α,ω-diiodoperfluoroalkanes. On the other hand, the treatment of (perfluoroalkyl)-p-tolyliodonium chlorides with silver sulfonates gave the iodonium benzenesulfonate 13, methanesulfonate 12, and triflate 14, and bisiodonium sulfate 15. Thermolysis of (perfluorooctyl)phenyliodonium triflate at about 150°C afforded perfluorooctyl triflate, iodobenzene, and (perfluorooctyl)iodobenzene in 73, 63, and 25% yields, respectively.

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