77479-01-7 Usage
Description
Methyl-3-[5-(2-methoxycarbonylethyl)pyrazin-2-yl]propionate is a complex organic compound with a unique chemical structure. It is characterized by its pyrazine and propionate functional groups, which contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Research:
Methyl-3-[5-(2-methoxycarbonylethyl)pyrazin-2-yl]propionate is used as a research compound for studying the pharmacological effects and chemical composition of organic acids derived from natural sources. Its application in this field is due to its potential to contribute to the development of novel therapeutic agents.
Used in the Study of Anti-tuberculosis Agents:
In the context of anti-tuberculosis research, Methyl-3-[5-(2-methoxycarbonylethyl)pyrazin-2-yl]propionate is used as a key compound in investigating the properties and efficacy of organic acids with anti-tuberculosis effects. This application is driven by the need to explore and develop new treatments for tuberculosis, a disease that continues to pose significant global health challenges.
Used in Chemical Synthesis:
Methyl-3-[5-(2-methoxycarbonylethyl)pyrazin-2-yl]propionate may also be used as an intermediate or building block in the synthesis of more complex organic molecules. Its unique structure and functional groups make it a valuable component in the development of new chemical entities with potential applications in various industries, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 77479-01-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,7 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77479-01:
(7*7)+(6*7)+(5*4)+(4*7)+(3*9)+(2*0)+(1*1)=167
167 % 10 = 7
So 77479-01-7 is a valid CAS Registry Number.
77479-01-7Relevant articles and documents
CONDENSATION PRODUCTS OF THE PORPHYRIN PRECURSOR 5-AMINOLEVULINIC ACID
Franck, Burchard,Stratmann, Helmut
, p. 919 - 923 (2007/10/02)
Condensation of the biogenetic porphyrin precursor 5-aminolevulinic acid (1) in alkaline solution yields besides some porphobilinogen (2) a dihydropyrazine (6) as the predominant product, which was isolated and characterized after dehydrogenation to the stable pyrazine (7a).This ends a longstanding uncertainty and reveals that the azomethine reaction, as can be expected for α-aminoketones, is strongly preferred by 5-aminolevulinic acid (1) under nonenzymatic conditions.A nor-porphobilinogen (9) was formed by condensation of a protected aminoacetoacetic ester with (1).
