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Thiocyanic acid, 4-[(4-nitro-1,3,5,7-cyclooctatetraen-1-yl)azo]phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106002-68-0

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106002-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106002-68-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,0,0 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 106002-68:
(8*1)+(7*0)+(6*6)+(5*0)+(4*0)+(3*2)+(2*6)+(1*8)=70
70 % 10 = 0
So 106002-68-0 is a valid CAS Registry Number.

106002-68-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ((1E,3E,5Z,7Z)-4-Nitro-cyclooctatetraenyl)-(4-thiocyanato-phenyl)-diazene

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:106002-68-0 SDS

106002-68-0Downstream Products

106002-68-0Relevant academic research and scientific papers

First examples of arylazo derivatives of cyclooctatetraene

Todres, Zori V.,Hovsepyan, Ghevork Ts.

, p. 747 - 750 (1997)

Disodium and dipotassium derivatives of 1,6-dinitrocyclooctatetraene (substrates) react with benzenediazo compounds (reagents) in THF to yield bis(azo)- or nitro(azo)-cyclooctatetraenes, the first cyclooctatetraene arylazo derivatives. Structures of the azo compounds are established by conventional methods and confirmed by X-ray crystallography. Together with the main products of electrophilic substitution, products of substrate-to-reagent electron transfer are formed. The electron-transfer products predominate with DMSO instead of THF as a solvent. The difference is apparently a result of ion-pair disintegration in the case of the substrate reactions when DMSO, a strong dissociating solvent, is used.

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