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26600-14-6

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26600-14-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26600-14-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,0 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 26600-14:
(7*2)+(6*6)+(5*6)+(4*0)+(3*0)+(2*1)+(1*4)=86
86 % 10 = 6
So 26600-14-6 is a valid CAS Registry Number.

26600-14-6SDS

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 2-ethenoxyethyl 3-phenylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Propenoic acid,3-phenyl-,2-(ethenyloxy)ethyl ester

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:26600-14-6 SDS

26600-14-6Downstream Products

26600-14-6Relevant articles and documents

VINYLOXYETHYL ESTERS OF MONOCARBOXYLIC ACIDS.

Mikhant'eva,Romanova,Mikhan'tev

, p. 1017 - 1022 (2007/10/02)

The authors examine methods of synthesis and the properties of 2-vinyloxyethyl acylates, a little-studied class of organic compounds on which literature information is very limited and which are of interest as possible monomers for synthesis of macromolecular compounds and as synthetic models of natural physiologically active substances. Methods have been devised for synthesis of 2-vinyloxyethyl acylates - potential monomers for synthesis of macromolecular and physiologically active compounds. The structural characteristics of the synthesized compounds were studied. Cationic polymerization of 2-vinyloxyethyl acylates was carried out, and the dependence of the reaction rate and of the properties of the resultant oligomers on the nature of the acyl radical was determined.

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