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72642-30-9

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72642-30-9 Usage

Uses

Fluorescent probe suitable for the study ofinterdiffusion of polymer latex

Check Digit Verification of cas no

The CAS Registry Mumber 72642-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72642-30:
(7*7)+(6*2)+(5*6)+(4*4)+(3*2)+(2*3)+(1*0)=119
119 % 10 = 9
So 72642-30-9 is a valid CAS Registry Number.

72642-30-9SDS

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-naphthalen-1-ylethyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-(1-naphthyl)ethyl methacrylate

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:72642-30-9 SDS

72642-30-9Downstream Products

72642-30-9Relevant articles and documents

Quantum amplified isomerization in polymers based on triplet chain reactions

Ferrar, Lorraine,Mis, Mark,Dinnocenzo, Joseph P.,Farid, Samir,Merkel, Paul B.,Robello, Douglas R.

, p. 5683 - 5692 (2008)

(Graph Presented) Photoinitiated triplet quantum amplified isomerizations (QAI) of substituted Dewar benzene derivatives in polymeric media are reported. The quantum efficiencies and the ultimate extents of reactant-to-product conversions increase significantly with the incorporation of appropriate co-sensitizers; compounds whose triplet energies are similar to or lower than that of the sensitizer and close to that of the reactant. These co-sensitizers serve to promote chain-propagating energy transfer processes and thereby increase the action sphere of photosensitization. Isomerization quantum yields increase, as predicted, with increasing concentrations of the reactants and the co-sensitizers. Chain amplifications as large as ~16 and extents of conversion that approach 100% have been achieved. Mechanistic schemes are proposed to account for the dynamics of the inherent energy transfer processes and provide a predictively useful model for the design of a new class of photoresponsive polymers based on changes in the refractive index of the materials.

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