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87597-22-6

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87597-22-6 Usage

General Description

Imidazo[1,2-a]pyrazine-2-carboxylic acid methyl ester is a chemical compound with potential pharmaceutical applications. It is a methyl ester derivative of imidazo[1,2-a]pyrazine-2-carboxylic acid, which is a heterocyclic compound. This chemical structure has been studied for its potential use in the development of pharmaceutical drugs, particularly in the context of medicinal chemistry and drug discovery. The compound's unique structure and potential biological activities make it an interesting candidate for further exploration in the field of drug development and therapeutic research.

Check Digit Verification of cas no

The CAS Registry Mumber 87597-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,5,9 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 87597-22:
(7*8)+(6*7)+(5*5)+(4*9)+(3*7)+(2*2)+(1*2)=186
186 % 10 = 6
So 87597-22-6 is a valid CAS Registry Number.

87597-22-6SDS

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 methyl imidazo[1,2-a]pyrazine-2-carboxylate

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:87597-22-6 SDS

87597-22-6Relevant articles and documents

Derives N-nitres et N-nitroses en serie tetrahydro-5,6,7,8 imidazopyrazinique : obtention et determination par RMN 1H des configurations Z et E.

Bonnet, Pierre-Antoine,Sablayrolles, Claire,Chapat, Jean-Pierre

, p. 468 - 480 (2007/10/02)

Les derives N-nitres et N-nitroses en serie tetrahydro-5,6,7,8 imidazopyrazinique sont obtenus simultanement lors de la nitration par HNO3 (d = 1.51) en milieu sulfurique.L'analyse des isomeres N-nitroses Z et E met en evidence l'apparition preponderante de la forme Z ainsi qu'une restriction importante a son equilibration.La stabilite particuliere de l'isomere Z est attribuee a l'existence d'une assistance electronique preferentielle entre groupement nitroso et protons en position 8.

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