56536-25-5

Upstream product

• 2010-06-2 2-Amino-4-phenylthiazole 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 

Downstream Products

• 62684-45-1 1-{[4-(4-methoxy-phenyl)-thiazol-2-ylamino]-(4-phenyl-thiazol-2-ylamino)-methyl}-naphthalen-2-ol 
• 62684-39-3 1-[bis-(4-phenyl-thiazol-2-ylamino)-methyl]-naphthalen-2-ol 
• 102764-23-8 Cu{C₆H₅(C₃HNS)NCH(C₁₀H₆)(O)}2 
• 56536-28-8 2-(2'-hydroxy-1-naphthyl)methylamino-4-phenyl-1,3-thiazole 

Relevant academic research and scientific papers

Synthesis of Schiff bases and oxazolidines from 2-amino-4-phenylthiazole

Reactions of 2-amino-4-phenylthiazole with aromatic aldehydes gave the corresponding Schiff bases which were reduced with sodium tetrahydridoborate to amines. Reactions of the Schiff bases with 2-methyloxirane, 2- chloromethyloxirane, and 2-phenoxymethylo

Synthesis and antioxidant activity of 2-amino-4-phenyl-1,3-thiazole derivatives

Azomethines and their hydrogenated derivatives were synthesized in the reaction of 2-amino-4-phenyl-1,3-thiazole with various hydroxyl-containing aldehydes. The synthesized compounds exhibit high antioxidant activity in the inhibited oxidation of cumene.

Synthetic, spectral, thermal and antibacterial studies on copper(II) and zinc(II) complexes using NNO donor Schiff bases

Copper(II) and zinc (II) complexes of Schiff bases, derived from substituted 2-aminothiazoles and o-hydroxyaldehydes, have been synthesized. The complexes are monomeric, possessing 1:2 (metal:lignad) stoichiometry and are non-electrolytic in nature. The Z

Ni(II), Cu(II) and Zn(II) Complexes of Tridentate Schiff Bases Derived from 4-Aryl-2-aminothiazoles

4-Aryl-2-aminothiazole and its substituted derivatives condense with substituted o-hydroxyaldehydes to form tridentate schiff bases (LH).These tridentate schiff bases form complexes of the type ML2 where M = Ni(II), Cu(II) or Zn(II).The elemental analyses