108735-87-1

Upstream product

• 20949-81-9 2-phenyl-thiazole-4-carbaldehyde 

Downstream Products

• 211948-78-6 2-phenyl-5-bromo-4-formyl-thiazole oxime 
• 1569318-94-0 C₁₉H₁₄N₂S₂ 
• 7113-14-6 2-phenylthiazole-4-carbothioamide 
• 10477-28-8 4,2'-diphenyl-[2,4']bithiazolyl 
• 7113-05-5 2-phenyl-1,3-thiazole-4-carbonitrile 
• 211948-80-0 5-Bromo-2-phenyl-thiazole-4-carbothioic acid amide 
• 211948-79-7 2-phenyl-5-bromo-4-cyano-thiazole 

Relevant academic research and scientific papers

The effect of some 4,2 and 5,2 bisthiazole derivatives on nitro-oxidative stress and phagocytosis in acute experimental inflammation

Nineteen bisthiazoles were tested in order to assess their anti-inflammatory and antioxidant properties. First, we evaluated the in vitro direct antioxidant capacity of the bisthiazoles using the DPPH radical scavenging method. Then, the anti-inflammatory

Hantzsch reaction intermediates as a means to obtain bisthiazoles and 5-acetyl-bisthiazoles

The synthesis, chemical and spectral data of some intermediates of Hantzsch's reaction is described. The synthesis of some 4-R-5-R1-2'-Aryl-2,4'-bisthiazoles was presented too. By interaction of acetic anhydride, hydroxythiasoline derivatives were converted to 5-acetyl-bisthiazoles.