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1022128-78-4

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1022128-78-4 Usage

General Description

N-(4-Methoxyphenyl)pyrazin-2-amine, also known as 2-Amino-4-methoxy-N-phenylpyrazine, is a chemical compound with the molecular formula C11H11N3O. It is a pyrazine derivative with a substituted amino group and a methoxyphenyl group. N-(4-Methoxyphenyl)pyrazin-2-amine is used in the pharmaceutical industry for the synthesis of various drugs and may have potential biological activities, such as anti-inflammatory and anticancer properties. Its precise uses and effects are still being studied and researched.

Check Digit Verification of cas no

The CAS Registry Mumber 1022128-78-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,2,1,2 and 8 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1022128-78:
(9*1)+(8*0)+(7*2)+(6*2)+(5*1)+(4*2)+(3*8)+(2*7)+(1*8)=94
94 % 10 = 4
So 1022128-78-4 is a valid CAS Registry Number.

1022128-78-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-Methoxyphenyl)pyrazin-2-amine

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

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More Details:1022128-78-4 SDS

1022128-78-4Downstream Products

1022128-78-4Relevant articles and documents

Palladium-Catalyzed Amination of Aryl Sulfides and Sulfoxides with Azaarylamines of Poor Nucleophilicity

Pratap, Ramendra,Yorimitsu, Hideki

, p. 2705 - 2712 (2019/06/19)

The amination of aryl sulfides and sulfoxides with azaarylamines is investigated using a palladium-N-heterocyclic carbene (NHC) complex. Because azaarylamines are less nucleophilic than anilines, more reactive diaryl sulfides and sulfoxides are found to be suitable coupling partners that liberate better leaving arenethiolate or arenesulfenate anions, instead of aryl methyl sulfides as reported previously.

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