80544-17-8 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-2-(Methoxycarbonylmethoxyimino)-2-(2-aminothiazol-4-yl)acetic acid is used as a potential active pharmaceutical ingredient for its possible antibacterial or antiviral properties, which could be leveraged in the development of new treatments for infectious diseases.
Used in Drug Synthesis:
As a building block in the synthesis of new drug candidates, (Z)-2-(Methoxycarbonylmethoxyimino)-2-(2-aminothiazol-4-yl)acetic acid contributes to the creation of novel compounds with potential therapeutic applications, expanding the range of available medications.
Used in Research and Development:
In the field of biological and chemical research, (Z)-2-(Methoxycarbonylmethoxyimino)-2-(2-aminothiazol-4-yl)acetic acid serves as a valuable research tool, aiding in the study of chemical interactions within biological systems and potentially uncovering new mechanisms of action for future drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 80544-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,4 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 80544-17:
(7*8)+(6*0)+(5*5)+(4*4)+(3*4)+(2*1)+(1*7)=118
118 % 10 = 8
So 80544-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N3O5S/c1-15-5(12)2-16-11-6(7(13)14)4-3-17-8(9)10-4/h3H,2H2,1H3,(H2,9,10)(H,13,14)/b11-6-
80544-17-8Relevant academic research and scientific papers
AN IMPROVED PROCESS FOR THE PREPARATION OF CEFIXIME
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Page/Page column 9, (2008/06/13)
There is provided an improved process for preparing cefixime. Thus, for example, 7-amino-3-vinyl-3-cephem-4-carboxylic acid is reacted with 2-mercapto-1,3-benzothiazolyl-(Z)-2-(2-aminothiazol-4-yl)-2-(methoxycarbonyl)-methoxyimino acetate in tetrahydrofuran and water at 4°C in the presence of triethylamine. The reaction mass is extracted with ethyl acetate. 7-[2-(2-Amino-4-thiazolyl)-2-(methoxycarbonylmethoxyimino)acetamido]-3-vinyl-3-cephem-4-carboxylic acid triethylamine salt present in the aqueous layer is hydrolyzed with sodium hydroxide in less than 30 minutes and aqueous hydrochloric acid is added immediately to adjust the pH to 4.8 to 5.2. Then, aqueous hydrochloric acid is added at 35°C to adjust the pH 2.5 and cooled to crystallize cefixime trihydrate in high purity.
