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Benzoic acid, 4-(1-oxido-2-quinoxalinyl)-, methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

922525-14-2

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922525-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 922525-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,2,5,2 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 922525-14:
(8*9)+(7*2)+(6*2)+(5*5)+(4*2)+(3*5)+(2*1)+(1*4)=152
152 % 10 = 2
So 922525-14-2 is a valid CAS Registry Number.

922525-14-2SDS

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 methyl 4-(1-oxidoquinoxalin-1-ium-2-yl)benzoate

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:922525-14-2 SDS

922525-14-2Downstream Products

922525-14-2Relevant academic research and scientific papers

Use of N-oxide compounds in coupling reactions

-

Page/Page column 13; 22, (2008/12/05)

Metal-catalyzed coupling process comprising reacting a compound of general formula 1 with a compound A-X, to obtain a compound of general formula 2, which may further be converted to a compound of general formula 3

Palladium-catalyzed cross-coupling reactions of diazine N-oxides with aryl chlorides, bromides, and iodides

Leclerc, Jean-Philippe,Fagnou, Keith

, p. 7781 - 7786 (2007/10/03)

New aspects of N-oxides: Pyrazine, pyridazine, and pyrimidine N-oxides are regioselectively arylated with aryl iodides, bromides, and chlorides in the presence of a palladium catalyst (see scheme). The resulting products can be deoxygenated in high yield

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