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2-Propenenitrile, 3-(4-acetylphenyl)-, (Z)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

115665-83-3

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115665-83-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115665-83-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,6 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 115665-83:
(8*1)+(7*1)+(6*5)+(5*6)+(4*6)+(3*5)+(2*8)+(1*3)=133
133 % 10 = 3
So 115665-83-3 is a valid CAS Registry Number.

115665-83-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (Z)-3-(4-acetylphenyl)acrylonitrile

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:115665-83-3 SDS

115665-83-3Downstream Products

115665-83-3Relevant academic research and scientific papers

First palladium-catalyzed Heck reactions with efficient colloidal catalyst systems

Beller, Matthias,Fischer, Hartmut,Kuehlein, Klaus,Reisinger,Herrmann

, p. 257 - 259 (1996)

For the first time it has been shown that palladium colloids are effective and active catalysts for the olefination of aryl bromides (Heck reaction). Worthy of note are the high activities of the catalyst system for activated aryl bromides under optimized reaction conditions, which are better than or comparable with classical palladium phosphine complexes. Addition of phosphines strongly retards the reaction rate of the colloid catalyst. Nevertheless, this type of catalyst is not suitable for the activation of non-activated substrates, especially technically interesting aryl chlorides.

Carbon-carbon cross-coupling reactions under continuous flow conditions using poly(vinylpyridine) doped with palladium

Mennecke, Klaas,Solodenko, Wladimir,Kirschning, Andreas

experimental part, p. 1589 - 1599 (2009/04/03)

Coordinative immobilization of an oxime-based pallada-cycle to poly(vinylpyridine)/glass composite materials shaped as Raschig rings or placed within the PASSflow microreactor affords technical devices that are well suited for performing palladium-catalyzed carbon-carbon cross-coupling reactions in the flow-through mode. Reusability of the immobilized precatalyst as well as applications in the microwave field were investigated. Experiments with thiol- and pyridine-based scavengers were carried out, which revealed that the active palladium species is likely to be composed of nanoparticles of unknown nature and that the poly(vinylpyridine) carrier has scavenging properties for these particles. Georg Thieme Verlag Stuttgart.

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