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Pyrazine, 2,5-bis(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24294-82-4

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24294-82-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24294-82-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,9 and 4 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24294-82:
(7*2)+(6*4)+(5*2)+(4*9)+(3*4)+(2*8)+(1*2)=114
114 % 10 = 4
So 24294-82-4 is a valid CAS Registry Number.

24294-82-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-bis(4-methoxyphenyl)pyrazine

1.2 Other means of identification

Product number -
Other names 2,5-Di-(4-methoxyphenyl)-pyrazin

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:24294-82-4 SDS

24294-82-4Downstream Products

24294-82-4Relevant academic research and scientific papers

Diarylpyrazine-based position isomers: A detailed study of optical properties and structure-property relationship

Gong, Young-Dae,Meti, Puttavva,Park, Dong-Jin

, (2020/02/11)

A versatile and expeditious synthetic route to pyrazine-based symmetric and asymmetric chromophores decorated with donor-acceptor (D-A) has been designed to study their structural effects on optical properties. Suzuki-Miyaura coupling of dihalopyrazine wi

The reaction of α-halocarbonyl compounds with (NH4)OH, (NH4)So4 or NH4CI solution under microwave-irradiation

Utsukihara, Takamitsu,Koshimura, Masahiro,Kitsuta, Kazunori,Sato, Akinori,Matsushita, Masatoshi,Takahashi, T. Tomoyoshi,Horiuchi, C. Akira

, p. 1495 - 1502 (2017/11/10)

Reaction of α-halo ketone (a-bromo ketone) under microwave, irradiation gives the pyrazine and quinoxaline derivative in good yields. This reaction affords a clean and convenient synthetic method for pyrazine and quinoxaline derivatives.

Highly efficient synthesis of 2,5-disubstituted pyrazines from (Z)-β-haloenol acetates

Chen, Zhengwang,Ye, Dongnai,Xu, Guohai,Ye, Min,Liu, Liangxian

supporting information, p. 6699 - 6702 (2013/10/01)

A highly efficient synthesis of a wide range of 2,5-disubstituted pyrazines from (Z)-β-haloenol acetates is described. The reactions are conducted under convenient conditions and provide products with excellent regioselectivity in moderate to excellent yields with a broad substrate scope, including a variety of aromatic and aliphatic haloenol acetates.

Microwave-assisted synthesis of α-hydroxy ketone and α-diketone and pyrazine derivatives from α-halo and α,α′-dibromo ketone

Utsukihara, Takamitsu,Nakamura, Hiroaki,Watanabe, Masashige,Akira Horiuchi

, p. 9359 - 9364 (2008/01/27)

A novel reaction of α-halo ketone (α-bromo and α-chloro ketone) with irradiation under microwave gave the corresponding α-hydroxyketone and pyrazine derivative in good yields. In the case of α,α′-dibromo ketone, α-diketone was obtained. This reaction affords a new, clean and convenient synthetic method for α-hydroxyketone, α-diketone, α-chloro ketone and pyrazine derivative.

Syntheses and Photophysical Properties of Some 5(2)-Aryl-2(5)-(4-pyridyl)oxazoles and Related Oxadiazoles and Furans

Hall, J. Herbert,Chien, Joseph Yuming,Kauffman, Joel M.,Litak, Peter T.,Adams, Jeffrey K.,et al.

, p. 1245 - 1273 (2007/10/02)

A number of 5-aryl-2-(4-pyridyl)oxazoles, a 2-aryl-5-(4-pyridyl)oxazole, the related oxadiazole and furan, several 2-(4-pyridyl)cycloalkanooxazoles, and many of their quaternary salts were prepared.No single standard synthesis was effective for preparation of more than a few of the 25 free bases described; methods often unique to a base were employed.Minor variations in structure sometimes produced large differences in absorption and emission wavelengths, as well as in the magnitude of the extinction coefficient.The salts are of interest as laser dyes, scintillation fluors, biological stains, and shifters for luminescent solar concentrators.

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