1192469-27-4

Basic information

• Product Name: 2-(3-chlorophenyl)-[1,2,4]triazolo[1,5-a]pyridine
• Synonyms: 2-(3-chlorophenyl)-[1,2,4]triazolo[1,5-a]pyridine
• CAS NO: 1192469-27-4
• Molecular Weight: 229.669
• Mol File: 1192469-27-4.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2-(3-chlorophenyl)-[1,2,4]triazolo[1,5-a]pyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-chlorophenyl)-[1,2,4]triazolo[1,5-a]pyridine(1192469-27-4)
• EPA Substance Registry System: 2-(3-chlorophenyl)-[1,2,4]triazolo[1,5-a]pyridine(1192469-27-4)

Safety Data

• Hazardous Substances Data: 1192469-27-4(Hazardous Substances Data)

Upstream product

• 504-29-0 2-aminopyridine 
• 827-64-5 ethyl 3-chlorobenzenecarboximidate hydrochloride 
• 1049977-96-9 C₁₂H₁₀ClN₃ 
• 766-84-7 3-chloro-benzonitrile 

Relevant articles and documents

Synthetic method 1, 2 and 4 - triazole compound

The invention discloses 1. 2,4 - Triazole compound synthesis method belongs to the technical field of synthesis of triazole compounds. After the reaction is finished, the reaction is carried out under the heating condition, and the target product 1, 2 and

Heterogeneous Copper(I)-Catalyzed Cascade Addition-Oxidative Cyclization of Nitriles with 2-Aminopyridines or Amidines: Efficient and Practical Synthesis of 1,2,4-Triazoles

The heterogeneous cascade addition-oxidative cyclization of nitriles with 2-aminopyridines or amidines was achieved in 1,2-dichlorobenzene or DMSO at 120-130 °C by using a 1,10-phenanthroline-functionalized MCM-41-supported copper(I) complex [Phen-MCM-41-

An efficient and recyclable heterogeneous catalytic system for the synthesis of 1,2,4-triazoles using air as the oxidant

Copper-zinc supported on Al2O3-TiO2 was found as a simple and efficient heterogeneous catalyst for the oxidative synthesis of 1,2,4-triazole derivatives using air as the green oxidant under ligand-, base- and additive-free conditions. The heterogeneous reactions carried out smoothly with a large range of substrates, including NO2-, vinyl-, pyrimidine- and imidazole-contained starting materials, and provided corresponding triazoles in moderate to excellent yields with low catalyst loading (1.6 mol%). Furthermore, the catalyst can be simply recycled many times without significant loss in catalytic activity. The Royal Society of Chemistry.