2-aminothiazole

2-aminothiazole

[¦tü ə‚mē·nō′thī·ə‚zȯl]
(organic chemistry)
C3H4N2S Pale-yellow crystals that melt at 92°C; soluble in cold water, slightly soluble in ethyl alcohol; used as an intermediate in the synthesis of sulfathiazole.
References in periodicals archive ?
Determination of Hg in water by CVAAS using 2-aminothiazole modified silica.
In view of the importance of 2-aminothiazole and its derivatives, several methods were reported in the literature.
The 2-aminothiazole and isatin were procured from local market.
Synthesis of 3-(thiazol-2-ylimino) indolin-2-one (3): An equimolar mixture of 2-aminothiazole and isatin were refluxed in methanol (40 mL) in presence of catalytic amount of glacial acetic acid for 3 h and allowed for cooling.
For this purpose, Schiff base 3 was prepared from acid catalyzed condensation of 2-aminothiazole and isatin.
8] have found that Schiff bases derived from 2-aminothiazole exhibit antibacterial, antifungal and anti- inflammatory activities.
Synthesis and Antitumor Activity Evaluation of some Schiff Bases Derived from 2-aminothiazole Derivatives.
Keywords: Multidrug resistance, Drug development, 2-Aminothiazole, Acylation of 2-aminothiazole, Antimicrobial activity.
In addition to this, 2-aminothiazole derivatives were converted to dithiocarbamate esters [27-29].
The screening results revealed that, the amide derived from 2-aminothiazole bearing the thiophene residue exhibited the highest inhibitory activity against Gram -ve Escherichia coli, Gram +ve Staphylococcus aureus and yeast Candida albicans.
To a cold solution of 2-aminothiazole (1a) or 2-amino-4-phenyl-thiazole (1b) (0.
Synthesis of 2-aminothiazoles and 2-thiazolecarboxamides with Anti-Anoxic Activity.