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6-Chloro-5-isobutyl-pyrazine-2-carboxylic acid amide is a complex chemical compound that belongs to the class of pyrazine derivatives. It is known for its potential therapeutic properties and is commonly used in research and pharmaceutical industries. 6-Chloro-5-isobutyl-pyrazine-2-carboxylic acid amide has been studied for its pharmacological activities, including its potential as an antifungal and antibacterial agent. Its unique chemical structure and potential therapeutic benefits make it an important compound in the field of medicinal chemistry and drug discovery.

182244-16-2

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182244-16-2 Usage

Uses

Used in Pharmaceutical Industry:
6-Chloro-5-isobutyl-pyrazine-2-carboxylic acid amide is used as a target for drug development due to its potential therapeutic properties and pharmacological activities.
Used in Research:
6-Chloro-5-isobutyl-pyrazine-2-carboxylic acid amide is used as a research compound for studying its potential as an antifungal and antibacterial agent, as well as its potential in the treatment of various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 182244-16-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,2,2,4 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 182244-16:
(8*1)+(7*8)+(6*2)+(5*2)+(4*4)+(3*4)+(2*1)+(1*6)=122
122 % 10 = 2
So 182244-16-2 is a valid CAS Registry Number.

182244-16-2Downstream Products

182244-16-2Relevant academic research and scientific papers

Synthesis and antituberculotic activity of 5-alkyl-6-chloro-2-pyrazinecarboxamides and corresponding thioamides

Hartl, Jiri,Dolezal, Martin,Krinkova, Jana,Lycka, Antonin,Odlerova, Zelmira

, p. 1109 - 1114 (2007/10/03)

Homolytic alkylation of 6-chloro-2-pyrazinecarbonitrile by alkanoic acid and subsequent partial hydrolysis afforded 5-alkyl-6-chloro-2-pyrazinecarboxamides 1a-1e. Reaction of amides 1a-1e by Lawesson's reagent afforded corresponding thioamides 2a-2e. The structure of compounds was confirmed by elemental analysis, IR and 1H NMR spectra. The assessment of in vitro antimycobacterial activity of the compounds was carried out. The highest antituberculotic activity against Mycobacterium tuberculosis and other mycobacterial strains in this series was shown by 5-(1,1-dimethylethyl)-6-chloro-2-pyrazinecarbothioamide (2e).

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