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1,2-Benzenedicarbonitrile, 3-[(2-ethylhexyl)oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

130107-88-9

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130107-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 130107-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,1,0 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130107-88:
(8*1)+(7*3)+(6*0)+(5*1)+(4*0)+(3*7)+(2*8)+(1*8)=79
79 % 10 = 9
So 130107-88-9 is a valid CAS Registry Number.

130107-88-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2-ethylhexoxy)benzene-1,2-dicarbonitrile

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:130107-88-9 SDS

130107-88-9Downstream Products

130107-88-9Relevant academic research and scientific papers

Method for preparing 3-alkoxyphtalocyanine

-

Page 3, (2008/06/13)

Production of a 3-alkoxyphthalo dinitrile by reaction of a 3-nitrophthalo dinitrile with an alcohol in a solvent other than one of the reactants and in presence of a base is such that either: (a) the 3-nitrophthalo dinitrile and the base are provided in a

Influence of substituents, reaction conditions and central metals on the isomer distributions of 1(4)-tetrasubstituted phthalocyanines

Rager, Christine,Schmid, Gabriele,Hanack, Michael

, p. 280 - 288 (2007/10/03)

The 1(4)- and 2(3)-tetraalkoxy-substituted nickel (5), copper (6), and metal-free phthalocyanines 7 and 8 were synthesized from the corresponding substituted phthalonitriles 2 and 4, respectively, and the four structural isomers formed for each phthalocya

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