67948-20-3

Upstream product

• 2103-91-5 2-amino-4-(p-methylphenyl)-1,3-thiazole 
• 90-02-8 salicylaldehyde 

Downstream Products

• 72192-81-5 4-(2-hydroxy-phenyl)-3-phenoxy-1-(4-p-tolyl-thiazol-2-yl)-azetidin-2-one 
• 67947-99-3 N-[2-(2-hydroxy-phenyl)-3-methyl-4-oxo-1-(4-p-tolyl-thiazol-2-yl)-azetidin-3-yl]-phthalimide 
• 77203-87-3 2-[(2-Hydroxy-phenyl)-(4-p-tolyl-thiazol-2-ylamino)-methyl]-cyclohexanone 
• 77204-00-3 2'-(2-Hydroxy-phenyl)-4-p-tolyl-[2,3']bithiazolyl-4'-one 
• 67947-84-6 N-[2-(2-hydroxy-phenyl)-4-oxo-1-(4-p-tolyl-thiazol-2-yl)-azetidin-3-yl]-phthalimide 
• 62684-50-8 2-[bis-(4-p-tolyl-thiazol-2-ylamino)-methyl]-phenol 
• 62684-53-1 2-[(4-phenyl-thiazol-2-ylamino)-(4-p-tolyl-thiazol-2-ylamino)-methyl]-phenol 
• 72192-80-4 3-(2-chloro-phenoxy)-4-(2-hydroxy-phenyl)-1-(4-p-tolyl-thiazol-2-yl)-azetidin-2-one 
• 72192-82-6 4-(2-hydroxy-phenyl)-3-(4-nitro-phenoxy)-1-(4-p-tolyl-thiazol-2-yl)-azetidin-2-one 
• 67948-14-5 N-[2-(2-hydroxy-phenyl)-3-isopropyl-4-oxo-1-(4-p-tolyl-thiazol-2-yl)-azetidin-3-yl]-phthalimide 

Relevant academic research and scientific papers

2-Hydroxybenzylidene-4-(4-SubstitutedPhenyl)-2-amino Thiazole and their Pt (II) complexes: Synthesis, characterization and biological study

Newly prepared Schiff bases; 2-Hydroxybenzylidene-4-x-phenyl)-2-aminothiazole,where x=H NO2 - CH3, -OCH3, –F, and -Cl (L1-L6), and their corresponding Pt (II) complexes (Pt(L1)s

Synthesis and Biological Activity of Some Schiff Bases Derived from Thiazoles and Benzothiazoles

4-Aryl-2-aminothiazoles and 2-aminobenzothiazoles undergo condensation with salicylaldehyde in the presence of piperidine to give the schiff bases II and III, respectively.A similar reaction of 4-aryl-2-aminothiazole methiodides gives the schiff bases 4-aryl-2-(2'-hydroxyaryliminomethyl)thiazole methiodides (IV).Several schiff bases have been condensed with cyclohexanone and thioglycollic acid to furnish 4-aryl-2-(2'-hydroxy-α-substituted benzylamino)thiazoles (V) and 2-(2'-hydroxyphenyl) or naphthyl)-3-(4''-arylthiazol-2''-yl)-4-thiazolidones (VI), respectively.Structure elucidation of the schiff bases has been made on the basis of their elemental analyses, IR and mass spectral data.The biological screening data of the schiff bases and their metal complexes are also presented.

Kinetics of Hydrolysis of N-Salicylidene-2-amino-4-substituted-phenylthiazoles

The kinetics of hydrolysis of schiff bases, N-salicylidene-2-amino-(4-substituted phenyl)thiazoles have been investigated in 20percent ethanol-water at 30.0 +/- 0.5 deg C, pH = 4.05-5.90 and I = 0.05 mol dm-3.The reaction proceeds via uncatalys