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82959-19-1

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82959-19-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82959-19-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,5 and 9 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82959-19:
(7*8)+(6*2)+(5*9)+(4*5)+(3*9)+(2*1)+(1*9)=171
171 % 10 = 1
So 82959-19-1 is a valid CAS Registry Number.

82959-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecan-2-one

1.2 Other means of identification

Product number -
Other names 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-HEPTADECA-FLUOROUNDECAN-2-ONE

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:82959-19-1 SDS

82959-19-1Downstream Products

82959-19-1Relevant articles and documents

NOVEL OXY-PERFLUOROALKYLATION

Umemoto, Teruo,Kuriu, Yuriko,Nakayama, Shin-ichi

, p. 4101 - 4102 (1982)

(Perfluoroalkyl)phenyliodonium sulfonates underwent novel oxy-perfluoroalkylation with alkenes under oxygen atmosphere in the presence of a base.

ELECTROCHEMICAL SYNTHESIS OF PERFLUOROALKYLACETONES

Vol'pin, I. M.,Kurykin, M. A.,Grinberg, V. A.,Vasil'ev, Yu. B.,German, L. S.

, p. 1395 - 1400 (2007/10/02)

The interaction of electrochemically generated radicals in the electrolysis of the perfluorocarboxylic acids RFCF2COOH (I), where RF = F (a), CF3 (b), C2F5 (c), C3F7 (d), C5F11 (e). and C7F15 (f), with isoprenyl acetate (II) was studied.The dependence of the results of the electrolysis on the adsorption capacity of the anode permits the proposition that the interaction of (II) with the ECG-radicals occurs close to the surface of the electrode.The yield of the perfluoroalkylacetones comprised 30-37percent.

A NEW METHOD FOR THE PREPARATION OF α-(PERFLUOROALKYL) CARBONYL AND γ-(PERFLUOROALKYL)-α,β-UNSATURATED CARBONYL COMPOUNDS

Umemoto, Teruo,Kuriu, Yuriko,Nakayama, Shin-ichi,Miyano, Osamu

, p. 1471 - 1474 (2007/10/02)

RfI(Ph)OSO2CF3 or RfI(Ph)OSO3H smoothly reacted with various trimethylsilyl enol ethers under mild conditions to give α(perfluoroalkyl) carbonyl and γ=)perfluoroalkyl)-α,β-unsaturated carbonyl compounds in high yields.

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