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20839-34-3

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20839-34-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20839-34-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,3 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 20839-34:
(7*2)+(6*0)+(5*8)+(4*3)+(3*9)+(2*3)+(1*4)=103
103 % 10 = 3
So 20839-34-3 is a valid CAS Registry Number.

20839-34-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl icos-5-enoate

1.2 Other means of identification

Product number -
Other names cis-5-Eicosensaeure-methylester

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:20839-34-3 SDS

20839-34-3Relevant articles and documents

-

Blum,S. et al.

, p. 3114 - 3120 (1972)

-

Polymers and surfactants on the basis of renewable resources

Warwel, Siegfried,Bruese, Falk,Demes, Christoph,Kunz, Michael,Klaas, Mark Ruesch gen

, p. 39 - 48 (2007/10/03)

A new strategy for the preparation of different polymers and special surfactants was developed. First, unsaturated fatty acid methyl esters obtained from plant oils were converted to terminally unsaturated esters and α-olefins by metathesis with ethylene using heterogeneous rhenium or homogeneous ruthenium catalysts. These esters were directly copolymerized with ethylene by an insertion-type palladium-catalyzed polymerization to functionalized polyolefins. Polyesters were synthesized by metathetical dimerization of ω-unsaturated esters and subsequent polycondensation of the produced internally unsaturated dicarboxylic esters or by acidic transesterification with petrochemical diols and additional acyclic diene metathesis polymerization, ω-epoxy fatty acid methyl esters, achieved by a new method of chemo-enzymatic epoxidation, were converted into polyethers with comb-structure catalyzed by aluminoxanes on the one hand and into sugar surfactants by nucleophilic ring-opening with amino carbohydrates on the other hand.

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