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PHENYL-(2-PYRIDIN-3-YL-PHENYL)-METHANONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159429-52-4

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159429-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159429-52-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,2 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 159429-52:
(8*1)+(7*5)+(6*9)+(5*4)+(4*2)+(3*9)+(2*5)+(1*2)=164
164 % 10 = 4
So 159429-52-4 is a valid CAS Registry Number.

159429-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name phenyl-(2-pyridin-3-ylphenyl)methanone

1.2 Other means of identification

Product number -
Other names Phenyl-(2-pyridin-3-yl-phenyl)-methanone

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:159429-52-4 SDS

159429-52-4Downstream Products

159429-52-4Relevant academic research and scientific papers

Efficient cross-coupling of functionalized arylzinc halides catalyzed by a nickel chloride-diethyl phosphite system

Gavryushin, Andrei,Kofink, Christiane,Manolikakes, Georg,Knochel, Paul

, p. 4871 - 4874 (2005)

(Chemical Equation Presented) The combination of diethyl phosphite and DMAP as ligands for nickel in an 8:1 THF-N-ethylpyrrolidinone (NEP) mixture allows a very efficient cross-coupling reaction to be performed between various functionalized arylzinc halides and aryl bromides, triflates and activated chlorides. The reaction proceeds at 25°C within 1-48 h and requires only 0.05 mol % of the nickel catalyst.

Nickel or Iron Catalysed Carbon-Carbon Coupling Reaction of Arylenes, Alkenes and Alkines

-

Page/Page column 5-6, (2010/08/07)

Organozinc compounds of the type R1—Ar1—ZnY (1) can be reacted with different functionalized aryl halides R2—Ar2—X (2) in the presence of catalytic amounts of Ni or Fe in a polar solvent or solvent mixture to form polyfunctional biaryles of the type R1—Ar1—Ar2—R2 (3). Organozinc compounds of the type (1) can be represented by the transmetallation reaction of functionalized aryl magnesium halides or lithium aryl compounds with e.g. ZnBr2.

An efficient Negishi cross-coupling reaction catalyzed by nickel(II) and diethyl phosphite

Gavryushin, Andrei,Kofink, Christiane,Manolikakes, Georg,Knochel, Paul

, p. 7521 - 7533 (2007/10/03)

A combination of diethyl phosphite-DMAP and Ni(II) salts forms a very effective catalytic system for the cross-coupling reactions of arylzinc halides with aryl, heteroaryl, and alkenyl bromides, chlorides, triflates, and nonaflates. The choice of solvent is quite important and the mixture of THF-N-ethylpyrrolidinone (NEP) (8:1) was found to be optimal. The reaction usually requires only 0.05 mol % of NiCl2 or Ni(acac)2 as catalyst and proceeds at room temperature within 1-48 h.

Inhibition of Myeloperoxidase Release from Rat Polymprphonuclear Leukocytes by a Series of Azachalcone Derivatives

Edwards, Michael L.,Stemerick, David M.,Sabol, Jeffrey S.,Diekema, Keith A.,Dinerstein, Robert J.

, p. 4357 - 4362 (2007/10/02)

A series of azachalcones was evaluated for ability to affect secretion of myeloperoxidase by rat polymorphonuclear leukocytes by fMLP.The compounds were found to interfere with cellular uptake of extracellular calcium.Structure-activity relationships are

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