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3-[1-[Difluoro[(trifluoroethenyl)oxy]methyl]-1,2,2,2-tetrafluoroethoxy]-2,2,3,3-tetrafluoropropanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69087-46-3

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69087-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69087-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,0,8 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 69087-46:
(7*6)+(6*9)+(5*0)+(4*8)+(3*7)+(2*4)+(1*6)=163
163 % 10 = 3
So 69087-46-3 is a valid CAS Registry Number.
InChI:InChI=1/C8HF13O4/c9-1(10)2(11)24-8(20,21)5(14,6(15,16)17)25-7(18,19)4(12,13)3(22)23/h(H,22,23)

69087-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3-tetrafluoro-3-[1,1,1,2,3,3-hexafluoro-3-(1,2,2-trifluoroethenoxy)propan-2-yl]oxypropanoic acid

1.2 Other means of identification

Product number -
Other names 2-Oxiranylmethyl 3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl ether

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:69087-46-3 SDS

69087-46-3Upstream product

69087-46-3Relevant academic research and scientific papers

Method of chlorination of end of fluorine-containing compound

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Page column 5, (2008/06/13)

There is provided a method of end-chlorination of a fluorine-containing compound which can easily provide a fluorine-containing monomer having a functional group such as nitrile group at relatively low cost. The method of chlorinating an end of a fluorine-containing compound having iodine atom at an end thereof comprises reacting a fluorine-containing organic compound having iodine atom at a molecular end thereof and represented by the formula (I): RfCX2I??(I) wherein Rf is an organic residue having fluorine atom, X is hydrogen atom or chlorine atom, with a chlorine gas at a temperature of from 150° C. to 180° C. under irradiation with light to cleave the C—I bond and replace iodine atom with chlorine atom.

Alkyl perfluoro-ω-fluoroformyl esters and monomers therefrom

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, (2008/06/13)

Alkyl perfluoro-ω-fluoroformyl esters are provided which have the formula STR1 wherein R is alkyl of 1-6 carbon atoms, and N IS 0-6 (PREFERABLY 0). Compounds where n is 0 are prepared by contacting SO3 with a compound of the formula Compounds where n is 1-6 are prepared by contacting a compound where n is 0 with hexafluoropropylene oxide. Also provided are polymerizable monomers having the formula STR2 wherein Y is --COOR, --COOH, --COOM or --CN, where M is an alkali metal, ammonium or quaternary ammonium and p is 1-5, prepared from alkyl perfluoro-ω-fluoroformyl esters of this invention.

Alkyl perfluoro-ω-fluoroformyl esters and their preparation

-

, (2008/06/13)

Alkyl perfluoro-ω-fluoroformyl esters are provided which have the formula: STR1 wherein R is alkyl of 1-6 carbon atoms, and n is 0-6 (preferably 0). Compounds where n is 0 are prepared by contacting SO3 with a compound of the formula ROOC--CF2 --CF2 --OR1. Compounds where n is 1-6 are prepared by contacting a compound where n is 0 with hexafluoropropylene oxide.

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