115437-26-8

Upstream product

• 108263-77-0 4-chloro-2-phenyl-thiazole-5-carbaldehyde 

Downstream Products

• 514806-50-9 (4-azido-2-phenyl-thiazol-5-yl)-methanol 
• 115437-61-1 5-<(N-p-tolylimino)methyl>-2-phenyl-4-<(triphenylphosphoranylidene)amino>thiazole 
• 115437-60-0 5-<(N-phenylimino)methyl>-2-phenyl-4-<(triphenylphosphoranylidene)amino>thiazole 
• 115437-66-6 5-(tolylimino)-2-phenyl-6-(p-meyhoxyphenyl)-5,6-dithiothiazolo<4,5-d>pyrimidines 
• 115437-64-4 5-(phenylimino)-2-phenyl-6-(p-methoxyphenyl)-5,6-dithiothiazolo-<4,5-d>pyrimidines 
• 115437-65-5 5-(tolylimino)-2-phenyl-6-tolyl-5,6-dithiothiazolo<4,5-d>pyrimidines 
• 115437-63-3 5-(phenylimino)-2-phenyl-6-tolyl-5,6-dithiothiazolo<4,5-d>pyrimidines 
• 115462-17-4 6-(4-Methoxy-phenyl)-2-phenyl-6H-thiazolo[4,5-d]pyrimidin-5-one 
• 115437-75-7 (5-Formyl-2-phenyl-thiazol-4-yl)-(4-methoxy-phenyl)-carbodiimide 
• 115437-70-2 2-Phenyl-6-p-tolyl-6H-thiazolo[4,5-d]pyrimidin-5-one 
• 115437-68-8 2-Phenyl-6-p-tolyl-6H-thiazolo[4,5-d]pyrimidine-5-thione 
• 115437-74-6 (5-Formyl-2-phenyl-thiazol-4-yl)-p-tolyl-carbodiimide 
• 115437-67-7 2,6-Diphenyl-6H-thiazolo[4,5-d]pyrimidine-5-thione 
• 115437-69-9 2,6-Diphenyl-6H-thiazolo[4,5-d]pyrimidin-5-one 

Relevant academic research and scientific papers

Neighbouring Group Effects on Rates of Thermolysis of 4-Azidothiazoles

Rate measurements for thermolysis of 4-azidothiazoles in p-xylene solution have identified neighbouring group effects from nitro (19-fold rate increase), phenyliminomethyl (16), formyl (4.5) and acetyl (2.2) substituents in the 5-position. These effects a

Fused Pyrimidines by a Tandem Aza-Wittig / Electrocyclic Ring Closure Strategy: Synthesis of Pyrazolo pyrimidyne, Triazolo pyrimidyne, and Thiazolo pyrimidyne Derivatives

The aza-Wittig reaction of iminophosphoranes derived from 5-azido -4-formylazoles or 4-azido-5-formylazoles with heterocumulenes leads to functionalized fused pyrimidines.Iminophosphoranes 12, derived from 5-azido-4-formylpyrazole, react under mild condit