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Ethanol, 2-(4-[2,2':6',2''-terpyridin]-4'-ylphenoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

127192-72-7

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127192-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127192-72-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,9 and 2 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 127192-72:
(8*1)+(7*2)+(6*7)+(5*1)+(4*9)+(3*2)+(2*7)+(1*2)=127
127 % 10 = 7
So 127192-72-7 is a valid CAS Registry Number.

127192-72-7SDS

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 2-[4-(2,6-dipyridin-2-ylpyridin-4-yl)phenoxy]ethanol

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:127192-72-7 SDS

127192-72-7Downstream Products

127192-72-7Relevant academic research and scientific papers

A green and straightforward synthesis of 4′-substituted terpyridines

Winter, Andreas,Van Den Berg, Antje M. J.,Hoogenboom, Richard,Kickelbick, Guido,Schubert, Ulrich S.

, p. 2873 - 2878 (2006)

A set of 4′-substituted 2,2′:6′,2″-terpyridines has been synthesized in a one-pot procedure under environmentally friendly reaction conditions using PEG and aqueous ammonia as solvents. This procedure features a short synthetic route, short reaction times, easy work-up, and good yields in comparison to conventional methods. The crystallographic data reveal the influence of the 4′-aryl substituent on the molecular structure and π-stacking behavior of the respective terpyridines. Georg Thieme Verlag Stuttgart.

PHARMACEUTICAL USE OF TERPYRIDINE DERIVATIVE

-

, (2008/06/13)

A terpyridine derivative represented by general formula (I) (wherein R represents hydrogen, (un)substituted phenyl, pyridyl, etc.), which has the effect of promoting the production of nerve growth factors or a neurotrophic factor activity. Hence it can be

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