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124311-28-0

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124311-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124311-28-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,1 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 124311-28:
(8*1)+(7*2)+(6*4)+(5*3)+(4*1)+(3*1)+(2*2)+(1*8)=80
80 % 10 = 0
So 124311-28-0 is a valid CAS Registry Number.

124311-28-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(Difluoro-undecafluorocyclohexyl-methoxy)-2,3,3,3-tetrafluoro-propionyl fluoride

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:124311-28-0 SDS

124311-28-0Relevant articles and documents

Novel perfluoroalkyl vinyl ether compound, process for preparing copolymer by using the compound, and optical plastic materials comprising copolymer prepared by the process

-

Page/Page column 6, (2008/06/13)

Disclosed herein are a novel perfluoroalkyl vinyl ether compound, a process for preparing a copolymer by using the perfluoroalkyl vinyl ether compound, and an optical plastic material comprising a copolymer prepared by the process. More specifically, the perfluoroalkyl vinyl ether has a particular molecular structure; the process is performed by copolymerizing the perfluoroalkyl vinyl ether compound with a common fluorinated olefin in the presence of a perfluorinated radical initiator; and, the optical plastic material comprises a copolymer prepared by the process and optionally a dopant. The copolymerization of the perfluoroalkyl vinyl ether with a common fluorinated olefin can provide a copolymer having a high molecular weight. In addition, appropriate control of the composition of the monomers can provide a completely amorphous copolymer. Since the polymer prepared by the process exhibits excellent thermal properties and is substantially transparent in the UV and near IR regions, it can be usefully applied to various optical plastic materials. Furthermore, a preform for a GI type plastic optical fiber fabricated by using the copolymer and the dopant has a high Tg, thus being stable, and a parabolic refractive index profile due to the presence of the dopant.

Polyfluoroalkyl Polyfluorovinyl Ethers. II. Synthesis of Perfluoro(cyclohexylmethyl) Perfluorovinyl Ether

Yuminov, V. S.

, p. 1040 - 1043 (2007/10/03)

Perfluoro(cyclohexylmethyl) perfluorovinyl ether was prepared by two methods: dehalogenation of perfluoro(cyclohexylmethyl) 2-iodotetrafluoroethyl ether and condensation of perfluorocyclohexylcarbonyl fluoride with perfluoropropene oxide, followed by thermolysis of the condensation product.

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