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87537-41-5

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87537-41-5 Usage

Type of compound

Heterocyclic compound

Components

Pyrazine ring and tolyl group

Usage

Flavoring agent in the food industry (nutty and earthy aroma), tobacco product flavoring, building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds

Physical form

Colorless to light yellow solid

Solubility

Sparingly soluble in water, soluble in organic solvents

Safety precautions

Handle with care and follow proper safety precautions when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 87537-41-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,3 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87537-41:
(7*8)+(6*7)+(5*5)+(4*3)+(3*7)+(2*4)+(1*1)=165
165 % 10 = 5
So 87537-41-5 is a valid CAS Registry Number.

87537-41-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-Methylphenyl)pyrazine

1.2 Other means of identification

Product number -
Other names o-Tolylaethersalicylsaeure

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:87537-41-5 SDS

87537-41-5Downstream Products

87537-41-5Relevant articles and documents

Electrochemical oxidation synergizing with Br?nsted-acid catalysis leads to [4 + 2] annulation for the synthesis of pyrazines

Liu, Kun,Song, Chunlan,Wu, Jiarong,Deng, Yuqi,Tang, Shan,Lei, Aiwen

supporting information, p. 765 - 769 (2019/02/27)

An electrochemical dehydrogenative [4 + 2] annulation for the synthesis of pyrazines has been developed under undivided electrolytic conditions. In this protocol, neither external chemical oxidants nor transition-metal catalysts are needed, and a wide range of substituted pyrazines could be obtained from simple ketones and diamines in high efficiencies. Of note is that this electrolysis could also be extended for the construction of biheteroarenes and large π systems with good yields.

Copper-catalysed cross-coupling of arylzirconium reagents with aryl and heteroaryl iodides

Thapa, Surendra,Basnet, Prakash,Gurung, Santosh K.,Giri, Ramesh

supporting information, p. 4009 - 4012 (2015/03/30)

An unprecedented CuI-catalysed cross-coupling of arylzirconium reagents with aryl and heteroaryl iodides is reported. Mechanistic studies with a Cp2ZrAr2 complex revealed that Cp2Zr(Ar)(Cl) is the reactive species that undergoes transmetalation with (PN-1)CuI. In addition, experiments with radical probes indicated that the reaction proceeds via a non-radical pathway. This journal is

A general catalyst for Suzuki-Miyaura and Sonogashira reactions of aryl and heteroaryl chlorides in water

Peng, Hui,Chen, Ya-Qin,Mao, Shu-Lan,Pi, Yun-Xiao,Chen, You,Lian, Ze-Yu,Meng, Tong,Liu, Sheng-Hua,Yu, Guang-Ao

supporting information, p. 6944 - 6952 (2014/09/29)

We report the synthesis of 2-(3-sulfonatomesityl)-5-sulfonatoindenyl) dicyclohexylphosphine hydrate sodium salt and its use in palladium-catalyzed Suzuki-Miyaura and Sonogashira coupling reactions in water (and biphasic water-organic solvent mixtures) to prepare a variety of functionalized biaryls and aryl alkynes in excellent yield. This journal is the Partner Organisations 2014.

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