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70592-07-3

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70592-07-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70592-07-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,9 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 70592-07:
(7*7)+(6*0)+(5*5)+(4*9)+(3*2)+(2*0)+(1*7)=123
123 % 10 = 3
So 70592-07-3 is a valid CAS Registry Number.

70592-07-3SDS

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-(4-chlorophenyl)ethene-1,1,2-triyl)tribenzene

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:70592-07-3 SDS

70592-07-3Downstream Products

70592-07-3Relevant articles and documents

Synthesis of Tetraarylethene Luminogens by C?H Vinylation of Aromatic Compounds with Triazenes

Doll, Martin,Fadaei-Tirani, Farzaneh,Ruggi, Albert,Scopelliti, Rosario,Severin, Kay,Suleymanov, Abdusalom A.

, p. 9957 - 9961 (2019/11/03)

Tetraarylethenes are obtained by acid-induced coupling of vinyl triazenes with aromatic compounds. This new C?H activation route for the synthesis of aggregation-induced emission luminogens is simple, fast, and versatile. It allows the direct grafting of triarylethenyl groups onto a variety of aromatic compounds, including heterocycles, supramolecular hosts, biologically relevant molecules, and commercial polymers.

An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins

Zhou, Chengxiang,Emrich, Daniel E.,Larock, Richard C.

, p. 1579 - 1582 (2007/10/03)

(Matrix presented) An efficient, regio- and stereoselective palladium-catalyzed route to tetrasubstituted olefins has been developed, which involves the intermolecular coupling of an aryl iodide, an internal alkyne, and an arylboronic acid. The reaction i

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