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105381-60-0

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105381-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105381-60-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,3,8 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 105381-60:
(8*1)+(7*0)+(6*5)+(5*3)+(4*8)+(3*1)+(2*6)+(1*0)=100
100 % 10 = 0
So 105381-60-0 is a valid CAS Registry Number.

105381-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E,E)-2,3-Dichlor-N,N'-dicyan-1,4-benzochinondiimin

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:105381-60-0 SDS

105381-60-0Relevant articles and documents

Multistep Reversible Redox Systems, XLVI. - N,N'-Dicyanoquinonediimines - A New Class of Compounds, I: Synthesis and General Properties

Aumueller, Alexander,Huenig, Siegfried

, p. 142 - 164 (2007/10/02)

A new class of quinone derivatives, the dicyanodiimines 2, 21, and 23, has been synthesized by the reaction of the corresponding quinones with bis(trimethylsilyl)carbodiimide (8) and titanium tetrachloride.A wide variety of substrates, even those which contain bulky groups and those which exhibit a strong influence on the redox potential, has been prepared.A route starting from p-phenylenediamines 4 via N,N'-dicyanodiamines 6 has been found to be much more limited.The spectroscopic properties of compounds 2, 21, and 23 are discussed with respect to their syn/anti isomerizations as well as substituent effects on their planarity.

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