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17650-46-3

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17650-46-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17650-46-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,5 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 17650-46:
(7*1)+(6*7)+(5*6)+(4*5)+(3*0)+(2*4)+(1*6)=113
113 % 10 = 3
So 17650-46-3 is a valid CAS Registry Number.

17650-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-ethoxycarbonyloxyethyl 2-methylprop-2-enoate

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:17650-46-3 SDS

17650-46-3Downstream Products

17650-46-3Relevant articles and documents

Novel monovinyl methacrylic monomers containing secondary functionality for ultrarapid polymerization: Steady-state evaluation

Berchtold, Kathryn A.,Nie, Jun,Stansbury, Jeffrey W.,Hacioglu, Bilge,Beckel, Eric R.,Bowman, Christopher N.

, p. 3165 - 3179 (2007/10/03)

Experimental investigations were made into the effects of monomer structure and functionality on free-radical polymerization kinetics. A more comprehensive understanding of how structural characteristics, monomer traits, and polymerization conditions influence the polymerization mechanisms and network evolution was desired. Variations in the nature of the monomers' secondary functionality and the terminal substitution were the primary variables examined. The three factors hypothesized as important to the advantageous polymerization characteristics observed are hydrogen bonding, hydrogen abstraction, and the electronic characteristics of the monomer. The experimental evaluations presented clearly demonstrate that each of these mechanisms contributes to the reactivity of these monomers and the networks that they form. The combination of these factors leads to cross-linked network formation and enhanced polymerization kinetics, i.e., monovinyl monomers with reactivities that rival those of commonly used divinyl monomers.

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