59134-92-8 Usage
Uses
Used in Pharmaceutical Industry:
2,2,2-Trifluoro-N-4-thiazolyl-acetamide is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties.
Used in Agrochemical Production:
In the agrochemical industry, 2,2,2-Trifluoro-N-4-thiazolyl-acetamide is used as an intermediate in the production of fungicides and insecticides, leveraging its biocidal properties to protect crops from pests and diseases.
Used in Anticancer Research:
2,2,2-Trifluoro-N-4-thiazolyl-acetamide is studied for its potential anticancer properties, with ongoing research exploring its effects on cancer cells and possible integration into cancer treatment strategies.
Used in Antifungal Applications:
As a fungicide, 2,2,2-Trifluoro-N-4-thiazolyl-acetamide is used to combat fungal infections in various settings, including agricultural and medical applications, due to its antifungal activity.
Used in Material Science:
2,2,2-Trifluoro-N-4-thiazolyl-acetamide is utilized in the development of new materials for various industrial applications, taking advantage of its chemical reactivity and structural characteristics to create innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 59134-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59134-92:
(7*5)+(6*9)+(5*1)+(4*3)+(3*4)+(2*9)+(1*2)=138
138 % 10 = 8
So 59134-92-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H3F3N2OS/c6-5(7,8)4(11)10-3-1-12-2-9-3/h1-2H,(H,10,11)
59134-92-8Relevant academic research and scientific papers
Mechanism of azo coupling reactions. Part 34. Reactivity of five-membered ring heteroaromatic diazonium ions
Diener, Heinz,Zollinger, Heinrich
, p. 1102 - 1107 (2007/10/02)
The azo coupling reactions of six five-membered heteroaromatic diazonium ions with 2-naphthol-3,6-disulfonic acid are investigated kinetically at various pH values.The dependence of the measured rate constants on the acidity of the aqueous reaction system is evaluated.It can be shown that the 2-naphtholate-3,6-disulfonate trianion reacts 4E8 - 8E8 times faster than the 2-naphthol-3,6-disulfonate dianion.The rate constants of the six diazonium ions vary by more than four orders of magnitude.The logarithms of the rate constants of all comparable diazonium ions correlate linearly with 1H-nmr chemical shifts of the respective unsubstituted heteroaromatic parent compounds.An analogous correlation was found for azo couplings with substituted benzenediazonium ions.Diazotization of heteroaromatic amines does not go to completion, rather to an equilibrium.It is shown therefore that in acidic coupling systems the azo compound is only the kinetically controlled product.The thermodynamic products are 1-nitroso-2-naphthol-3,6-disulfonic acid and the heteroaromatic amine.
4-Aminothiazole
-
, (2008/06/13)
4-Aminothiazole is prepared in stable useful form by alkaline hydrolysis of 4-trifluoroacetamidothiazole. Also prepared are 4-sulfathiazole and 2-(4-thaizolyl)-indazole.
