20721-18-0 Usage
Description
2-Hydroxy-6-methylpyrazine is an organic compound that serves as a valuable synthetic intermediate in the chemical industry. It is characterized by its unique molecular structure, which features a pyrazine ring with a hydroxyl group at the 2nd position and a methyl group at the 6th position. 2-HYDROXY-6-METHYLPYRAZINE plays a significant role in the synthesis of various pharmaceuticals and other organic compounds.
Uses
Used in Pharmaceutical Synthesis:
2-Hydroxy-6-methylpyrazine is used as a synthetic intermediate for the production of 2-hydroxy-3-phenyl-6-methylpyrazine, which is a compound of interest in the pharmaceutical industry. This intermediate is crucial for the development of new drugs and therapeutic agents.
Used in Analytical Chemistry:
In the field of analytical chemistry, 2-hydroxy-6-methylpyrazine serves as a fluorescent degradation product of the antibiotic cephalexin. It is utilized for the determination of cephalexin in aqueous solutions and human plasma, providing a reliable method for monitoring the presence and concentration of this antibiotic in various samples.
Used in Research and Development:
2-Hydroxy-6-methylpyrazine is also employed in research and development settings, where it is used to explore its potential applications and properties. This includes studying its chemical reactivity, stability, and interactions with other compounds, which can lead to the discovery of new applications and uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 20721-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,7,2 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 20721-18:
(7*2)+(6*0)+(5*7)+(4*2)+(3*1)+(2*1)+(1*8)=70
70 % 10 = 0
So 20721-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H5ClN2/c1-4-2-7-3-5(6)8-4/h2-3H,1H3
20721-18-0Relevant articles and documents
Emimycin and its nucleoside derivatives: Synthesis and antiviral activity
Plebanek, Elzbieta,Lescrinier, Eveline,Andrei, Graciela,Snoeck, Robert,Herdewijn, Piet,De Jonghe, Steven
, p. 93 - 103 (2017/12/26)
The synthesis of emimycin, 5-substituted emimycin analogues and the corresponding ribo- and 2′-deoxyribonucleoside derivatives is described. Emimycin, its 5-substituted congeners and the ribonucleoside derivatives are completely devoid of antiviral activity against RNA viruses. In contrast, some of the 2′-deoxyribosyl emimycin derivatives are potent inhibitors of the replication of herpes simplex virus-1 and varicella-zoster virus, lacking cytotoxicity.
