29676-71-9 Usage
Description
2-Aminothiazol-4-acetic acid is a light orange powder with almost white to light beige crystalline properties. It is an organic compound that has been utilized in various applications due to its unique chemical properties.
Uses
Used in Electrochemistry:
2-Aminothiazol-4-acetic acid is used as a component in the preparation of poly(2-amino-4-thiazoleacetic acid)/multiwalled carbon nanotubes modified glassy carbon electrodes. This application is for the voltammetric determination of copper ions, allowing for efficient and accurate measurement of copper ion concentrations.
Used in Polymer Synthesis:
In the field of polymer chemistry, 2-aminothiazol-4-acetic acid serves as a monomer for the electrochemical synthesis of novel thiozole-based copolymers. These copolymers exhibit unique properties and have potential applications in various industries.
Used in Coordination Chemistry:
2-Aminothiazol-4-acetic acid is utilized in the preparation of aquabis(2-amino-1,3-thiazole-4-acetato-κ2O,N3)nickel (II), a coordination compound. 2-Aminothiazol-4-acetic acid has potential applications in catalysis, materials science, and other fields where coordination complexes are of interest.
Overall, 2-aminothiazol-4-acetic acid is a versatile compound with applications in electrochemistry, polymer synthesis, and coordination chemistry, making it a valuable asset in scientific research and industrial applications.
Air & Water Reactions
Insoluble in water.
Fire Hazard
Flash point data for 2-Aminothiazol-4-acetic acid are not available. 2-Aminothiazol-4-acetic acid is probably combustible.
Check Digit Verification of cas no
The CAS Registry Mumber 29676-71-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,6,7 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29676-71:
(7*2)+(6*9)+(5*6)+(4*7)+(3*6)+(2*7)+(1*1)=159
159 % 10 = 9
So 29676-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C5H6N2O2S/c6-5-7-3(2-10-5)1-4(8)9/h2H,1H2,(H2,6,7)(H,8,9)/p-1
29676-71-9Relevant articles and documents
Synthesis, characterization and antitumor activity of Cu(II), Co(II), Zn(II) and Mn(II) complex compounds with aminothiazole acetate derivative
Alexandru, Maria-Gabriela,Velickovic, Tanja Cirkovic,Jitaru, Ioana,Grguric-Sipka, Sanja,Draghici, Constantin
, p. 639 - 645 (2010)
This paper presents the synthesis of complex compounds of type [M(L1)2], where M(II)= Cu (1), Co (2), Zn (3), L1=2-aminothiazole-4-acetate and [Mn(L1)2(H2O)] (4) using ethyl 2-(2-aminothiazole-4-yl) acetate (L), and characterization by elemental analysis, magnetic susceptibilities, IR, 1H-NMR, UV-Vis spectroscopy and for [Mn(L1)2(H2O)] also by X-ray diffraction. In vitro cytotoxicity studies were performed on human cervix adenocarcinoma, HeLa cells. The antitumor selectivity was assessed using normal human peripheral blood mononuclear cells, PBMC as control. Versita Sp. z o.o.
One-pot method for preparing cefotiam intermediate 2-aminothiazole-4-acetic acid
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Paragraph 0041; 0043, (2020/08/25)
The invention discloses a one-pot method for preparing a cefotiam intermediate that is 2-aminothiazole-4-acetic acid. The method is technically characterized by comprising the following steps: 1) by taking water as a solvent, carrying out ring closing by using thiourea and ethyl 4-chloroacetoacetate at a proper temperature and a proper molar ratio to generate ethyl 2-aminothiazole-4-acetate; afterthe reaction is finished, directly carrying out the next step of reaction on the reaction solution; 2) adding a certain amount of an alkali into the reaction solution for a hydrolysis reaction at a proper temperature, and 3) after the reaction is finished, adding a certain amount of an acid into the reaction solution at a proper temperature to adjust the pH value, and separating out the product.
Thiazole, imidazole and oxazole compounds and treatments of disorders associated with protein aging
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, (2008/06/13)
Provided are, among other things, compounds of formula I or IA, . Also provided are methods of treatment with such compounds.