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2-IODO-TEREPHTHALONITRILE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18870-14-9

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18870-14-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18870-14-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,8,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18870-14:
(7*1)+(6*8)+(5*8)+(4*7)+(3*0)+(2*1)+(1*4)=129
129 % 10 = 9
So 18870-14-9 is a valid CAS Registry Number.

18870-14-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodobenzene-1,4-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 2-Jod-terephthalonitril

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:18870-14-9 SDS

18870-14-9Relevant academic research and scientific papers

INHIBITORS OF BETA-SECRETASE

-

Page/Page column 62-63, (2011/09/30)

The present invention relates to compounds represented by Structural Formula (I) or a pharmaceutically acceptable salt thereof. Definitions for the variables are provided herein.

Carbopalladation of nitriles: Synthesis of 2,3-diarylindenones and polycyclic aromatic ketones by the Pd-catalyzed annulation of alkynes and bicyclic alkenes by 2-iodoarenenitriles

Pletnev, Alexandre A.,Tian, Qingping,Larock, Richard C.

, p. 9276 - 9287 (2007/10/03)

2-Iodobenzonitrile, its derivatives, and various heterocyclic analogues undergo palladium(O)-catalyzed annulation onto diarylacetylenes or bicyclic alkenes to afford 2,3-diarylindenones and polycyclic aromatic ketones in very good to excellent yields. This reaction represents one of the first examples of the addition of an organopalladium moiety to the carbon-nitrogen triple bond of a nitrile. The reaction is compatible with a number of functional groups. A reaction mechanism, as well as a model accounting for the electronic effects of substituents on the aromatic ring of the nitrile, is proposed.

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