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1,1,2,2-Ethanetetracarbonitrile, 1,2-bis(4-methylphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

34404-77-8

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34404-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34404-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,4,0 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 34404-77:
(7*3)+(6*4)+(5*4)+(4*0)+(3*4)+(2*7)+(1*7)=98
98 % 10 = 8
So 34404-77-8 is a valid CAS Registry Number.

34404-77-8SDS

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 1,2-bis(4-methylphenyl)ethane-1,1,2,2-tetracarbonitrile

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:34404-77-8 SDS

34404-77-8Relevant academic research and scientific papers

Effect of Substituents on the Bond Strength of Air-Stable Dicyanomethyl Radical Thermochromes

Peterson, Joshua P.,Geraskina, Margarita R.,Zhang, Rui,Winter, Arthur H.

, p. 6497 - 6501 (2017/06/23)

A series of substituted aryl dicyanomethyl radicals were synthesized, and the bonding thermodynamic parameters for self-dimerization were determined from van't Hoff plots obtained from variable-temperature electron paramagnetic resonance and ultraviolet-v

CARBON-CARBON BOND FORMATION BY COORDINATION OF CARBOCATIONS WITH CARBANIONS.

Arnett, Edward M.,Troughton, E. B.

, p. 3299 - 3302 (2007/10/02)

Direct attack of resonance-stabilized carbenium ions and carbanions can be regulated to provide a wide range of rates and equilibria for the study of carbon-carbon bond formation.

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