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Upstream product

• 64310-34-5 3-(p-methylphenyl)-5-mercapto-4H-1,2,4-triazole 
• 70-11-1 α-bromoacetophenone 
• 87614-19-5 N-(4-phenylthiazole-2-yl)p-tolylimidoyl chloride 
• 87614-00-4 2-p-methylbenzoylamino-4-phenylthiazole 
• 874-60-2 4-methyl-benzoyl chloride 
• 2010-06-2 2-Amino-4-phenylthiazole 
• 103966-09-2 1-(4-phenylthiazol-2-yl)-5-p-tolyltetrazole 
• 86812-45-5 1-Phenyl-2-(5-p-tolyl-4H-[1,2,4]triazol-3-ylsulfanyl)-ethanone 

Relevant academic research and scientific papers

Synthesis of 2,5-Diarylthiazolo-s-triazoles

2,5-Diarylthiazolo-s-triazoles (II) have been synthesised via 1-(4-arylthiazol-2-yl)-5-aryltetrazoles (VII).Compounds (VII) have been synthesised by the reaction of 2-aroylamino-4-arylthiazoles (V) with phosphorus pentachloride, and azidolysis of t

Heterocyclic Systems Containing Bridgehead Nitrogen Atoms: Part XLV - Reaction of 5-Mercapto-3-p-tolyl-s-triazole with α,β-Bifunctional Compounds

5-Mercapto-3-p-tolyl-s-triazole (II) on condensation with α-halogenoketones and subsequent cyclization of the intermediate ketones (III) with PPA furnishes the corresponding thiazolo-s-triazoles (IV) and not the isomeric thiazolo-s-triazoles

Heterocyclic Systems Containing Bridgehead Nitrogen Atom: Syntheses of Thiazolo-s-triazoles & Isomeric Thiazolo-s-triazole

The reaction of 3-p-tolyl-5-mercapto-s-triazole (II) with α-haloketones in dry methanol gives thiazolo-s-triazole (III) derivatives in one-step and not the isomeric thiazolo-s-triazole (V) derivatives.Unequivocal synthesis of latter has also