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Pyrazine, 2,5-dimethyl-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

106860-97-3

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106860-97-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106860-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,8,6 and 0 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 106860-97:
(8*1)+(7*0)+(6*6)+(5*8)+(4*6)+(3*0)+(2*9)+(1*7)=133
133 % 10 = 3
So 106860-97-3 is a valid CAS Registry Number.

106860-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethyl-3-phenylpyrazine

1.2 Other means of identification

Product number -
Other names Pyrazine,2,5-dimethyl-3-phenyl

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:106860-97-3 SDS

106860-97-3Relevant academic research and scientific papers

Iron catalyzed cross coupling reactions of aromatic compounds

-

Page/Page column 16, (2010/02/03)

A process for the production of compounds Ar—R1 by means of a cross-coupling reaction of an organometallic reagent R1—M with an aromatic or heteroaromatic substrate Ar—X catalyzed by one or several iron salts or iron complexes as catalysts or pre-catalysts, present homogeneously or heterogeneously in the reaction mixture. This new invention exhibits substantial advantages over established cross coupling methodology using palladium- or nickel complexes as the catalysts. Most notable aspects are the fact that (i) expensive and/or toxic nobel metal catalysts are replaced by cheap, stable, commercially available and toxicologically benign iron salts or iron complexes as the catalysts or pre-catalysts, (ii) commercially attractive aryl chlorides as well as various aryl sulfonates can be used as starting materials, (iii) the reaction can be performed under “ligand-free” conditons, and (iv) the reaction times are usually very short.

Iron-catalyzed cross-coupling reactions

Fuerstner, Alois,Leitner, Andreas,Mendez, Maria,Krause, Helga

, p. 13856 - 13863 (2007/10/03)

Simple iron salts such as FeCln, Fe(acac)n (n = 2,3) or the salen complex 4 turned out to be highly efficient, cheap, toxicologically benign, and environmentally friendly precatalysts for a host of cross-coupling reactions of alkyl o

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