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

22248-24-4

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22248-24-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22248-24-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,4 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 22248-24:
(7*2)+(6*2)+(5*2)+(4*4)+(3*8)+(2*2)+(1*4)=84
84 % 10 = 4
So 22248-24-4 is a valid CAS Registry Number.

22248-24-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-methoxyphenyl)ethane-1,1,2-tricarbonitrile

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:22248-24-4 SDS

22248-24-4Relevant academic research and scientific papers

New Cyanoarylporphyrazines with High Sensitivity of Photophysical Parameters to Viscosity as Promising Agents for Photodynamic Therapy

Balalaeva, I. V.,Boyarskii, V. P.,Klapshina, L. G.,Ladilina, E. Yu.,Lermontova, S. A.,Lyubova, T. S.,Plekhanov, V. I.

, p. 249 - 256 (2020/04/20)

Abstract: Photophysical properties and photodynamic activity for a series of cyanoarylporphyrazine pigments have been analyzed depending on the nature of the substituents and their position in the aromatic ring. Replacement of the fluorine atom in the par

Synthesis of Polyfunctionalized Pyrroles via a Tandem Reaction of Michael Addition and Intramolecular Cyanide-Mediated Nitrile-to-Nitrile Condensation

Guchhait, Sankar K.,Sisodiya, Shailendra,Saini, Meenu,Shah, Yesha V.,Kumar, Gulshan,Daniel, Divine P,Hura, Neha,Chaudhary, Vikas

, p. 5807 - 5815 (2018/05/05)

A new approach for the synthesis of tetrasubstituted/functionalized NH-pyrroles from gem-diactivated acrylonitriles and TMSCN has been developed. The strategy utilizes the generation of vic-dinitrile via Michael addition and cyanide-mediated nitrile-to-nitrile cyclocondensation, which proceed in tandem guided by manifold roles of CN . An extended application to the production of fused pyrrole has also been realized.

Sizeable red-shift of absorption and fluorescence of subporphyrazine induced by peripheral push and pull substitution

Liang, Xu,Shimizu, Soji,Kobayashi, Nagao

supporting information, p. 13781 - 13784 (2014/12/11)

Peripheral substitution with electron-donating (push) and electron-withdrawing (pull) substituents caused a sizeable red-shift of the Q band absorption and fluorescence of subporphyrazine, and the red-shift was controlled by the push substituents. Control

Synthesis and Trasformations of 5-Amino-2,3-dihydro-oxoles

Ciller, J. A.,Martin, M.,Quinteiro, M.,Seoano, C.,Soto, J. L.

, p. 1321 - 1331 (2007/10/02)

Treatment of α-cyanocinnamonitriles 1 with hydrogen cyanide in acetone results in the formation of 5-amino-2,3-dihydro-oxoles 3.Tricyanoethanes 2 can be obtained as intermediate compounds in a two-step process leading to the same dihydro-oxoles.Acid hydro

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