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3198-30-9

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3198-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3198-30-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,9 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3198-30:
(6*3)+(5*1)+(4*9)+(3*8)+(2*3)+(1*0)=89
89 % 10 = 9
So 3198-30-9 is a valid CAS Registry Number.

3198-30-9SDS

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 terephthalate(2-)

1.2 Other means of identification

Product number -
Other names 1,4-dicarboxybenzene

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:3198-30-9 SDS

3198-30-9Upstream product

3198-30-9Relevant articles and documents

An Electrode-Supported Oxidation Catalyst Based on Ruthenium(IV). pH "Encapsulation" in a Polymer Film

Samuels, George J.,Meyer, Thomas J.

, p. 307 - 312 (1981)

The known oxidative catalytic behavior of ions (bpy)2(py)RuO2+ (bpy is 2,2'-bipyridine; py is pyridine) and (trpy)(bpy)RuO2+ (trpy is 2,2',2''-terpyridine) has been successfully transferred to electrode surfaces.The electrodes were chemically modified by deposition of thin polymeric films containing the (bpy)2(H2O)RuII group bound to poly-4-vinylpyridine.Upon oxidation to RuIV on the surface, catalytic oxidation currents are observed for the modified electrodes in the presence of 2-propanol, p-toluic acid, and the xylenes with an added surfactant.The effective catalytic lifetimes of the films are limited (>30 turnovers per redox site) by a competing reaction within the polymer film which changes the nature of the redox sites.An unusual pH effect has been observed in the polymer films.Below pH 4, potentials measured by cyclic voltammetry for the bound III(py)(*)>2+/II(py)(*)>2+ and IV(py)(*)>2+/III(py)(*)>2+ couples change with pH as expected.Above pH 4, where the unbound pyridyl groups in the polymer become deprotonated, up to pH 9.2 the redox couples no longer respond to pH changes in the bulk solution.The difference in the pH behavior between the polymer in solution and on the electrode surface has allowed us to observe the deposition process by cyclic voltammetry.In acid solution, the polymer film is open and large amounts of ferri- or ferrocyanide ions can be incorporated reversibly into the films by ion exchange.Over a longer time period, the cyano ions are permanently bound in the films, apparently by the formation of a cyano-bridged Fe-Ru dimer.

Novel Electrocatalytic Procedure for the Oxidation of Alcohols, Aldehydes, Cyclic Ketones, and C-H Bonds Adjacent to Olefinic or Aromatic Groups

Thompson, Mark S.,Giovani, Wagner F. De,Moyer, Bruce A.,Meyer, Thomas J.

, p. 4972 - 4977 (2007/10/02)

A novel electrocatalytic procedure is described for the oxidation of primary and secondary alcohols, cyclic ketones, and C-H bonds adjacent to aromatic or olefinic groups.The procedure involves the use of the RuIVoxidant 2+ (trpy is 2,2',2''-terpyridine; bpy is 2,2'-bipyridine) in water at pH 6.8 or in dimethyl sulfone-water mixtures and is based on a electrochemical "shuttle" mechanism in which the RuIV complex is regenerated by electrochemical oxidation of II(trpy)(bpy)(H2O)>2+.

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