110130-88-6 Usage
Uses
Used in Pharmaceutical Industry:
(Z)-2-(2-AMINOTHIAZOL-4-YL)-2-ACETYLOXYIMINOACETIC ACID is used as a pharmaceutical intermediate for the development of new drugs. Its biological activities, including antibacterial and antioxidant properties, make it a valuable component in the creation of medications targeting various diseases and conditions.
Used in Biochemical Research:
In the field of biochemistry, (Z)-2-(2-AMINOTHIAZOL-4-YL)-2-ACETYLOXYIMINOACETIC ACID serves as a research tool to study biochemical processes. Its unique structure allows scientists to explore its interactions with other molecules and enzymes, potentially leading to a better understanding of biological mechanisms and the development of novel therapeutic strategies.
Used in Antimicrobial Agents:
(Z)-2-(2-AMINOTHIAZOL-4-YL)-2-ACETYLOXYIMINOACETIC ACID is utilized as an antimicrobial agent due to its demonstrated antibacterial properties. It can be incorporated into formulations to combat bacterial infections, offering an alternative or adjunct to existing treatments.
Used in Antioxidant Formulations:
Leveraging its antioxidant properties, (Z)-2-(2-AMINOTHIAZOL-4-YL)-2-ACETYLOXYIMINOACETIC ACID is used in antioxidant formulations to protect cells from oxidative damage. This application is particularly relevant in the development of nutraceuticals and cosmeceuticals aimed at promoting health and wellness.
Check Digit Verification of cas no
The CAS Registry Mumber 110130-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,1,3 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 110130-88:
(8*1)+(7*1)+(6*0)+(5*1)+(4*3)+(3*0)+(2*8)+(1*8)=56
56 % 10 = 6
So 110130-88-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O4S/c1-3(11)14-10-5(6(12)13)4-2-15-7(8)9-4/h2H,1H3,(H2,8,9)(H,12,13)/b10-5+
110130-88-6Relevant articles and documents
Preparation method of aminothiazole acetyloxime acid with controllable particle size
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Paragraph 0038; 0040-0041; 0042; 0044-0045; 0046; 0048-0049, (2021/04/14)
The invention relates to a preparation method of aminothiazole acetyloxime acid with a controllable particle size, and belongs to the technical field of chemical pharmacy. The preparation method comprises the following steps: ahydrolysis step: hydrolyzing ethyl 2-(2-aminothiazole-4-yl)-2-hydroxyiminoacetate serving as a raw material to generate a compound 1; an acylation step: dropwisely adding an acylating agent into the system to perform acylation reaction to obtain a compound 2; and a crystallization step: adding activated carbon into the reaction system for decolorization, then dropwise adding an acidic solution into the system at different temperatures to control the pH value of the system, and after the solid is separated out, carrying out centrifugal drying to obtain a compound 3 with controllable particle size. According to the method, by controlling different acid liquor adding temperatures, the particle size of the prepared aminothiazole acetyloxime acid is controllable; and the technological process is simple to operate and suitable for industrial production.
A CEFDINIR INTERMEDIATE
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Page 10-11, (2010/02/06)
7-[2-(2-aminothiazol-4-yl)-2-(methylcarbonyloxyimino)acetamido]-3-vinyl-cephem-4-carboxylic acid of formula (I), in the form of a crystalline salt and use thereof, e.g. in the preparation of pure cefdinir. In another aspect this invention relates to the c
PROCESS FOR PRODUCING ANHYDRIDE OF AMINOTHIAZOLE DERIVATIVE
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, (2008/06/13)
This invention provides a novel industrial process for preparation of an anhydride of 2-(2-aminothiazole-4-yl)-2-hydroxy compound.
