756819-68-8

Basic information

• Product Name: 4H-1,2,4-Triazole,4-cyclohexyl-3-methyl-(9CI)
• Synonyms: 4H-1,2,4-Triazole,4-cyclohexyl-3-methyl-(9CI)
• CAS NO: 756819-68-8
• Molecular Formula: C9H15N3
• Molecular Weight: 165.2355
• Product Categories: AMINETERTIARY
• Mol File: 756819-68-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4H-1,2,4-Triazole,4-cyclohexyl-3-methyl-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,2,4-Triazole,4-cyclohexyl-3-methyl-(9CI)(756819-68-8)
• EPA Substance Registry System: 4H-1,2,4-Triazole,4-cyclohexyl-3-methyl-(9CI)(756819-68-8)

Safety Data

• Hazardous Substances Data: 756819-68-8(Hazardous Substances Data)

Upstream product

• 3451-51-2 2-methyl-[1,3,4]-oxadiazole 
• 108-91-8 cyclohexylamine 
• 766-93-8 N-cyclohexylformamide 
• 20635-13-6 N-cyclohexylmethanethioamide 
• 1068-57-1 acetic acid hydrazide 
• 756819-70-2 N-[(E)-dimethylaminomethylideneamino]acetamide 
• 1124-53-4 N-cyclohexylacetamide 

Relevant articles and documents

Tunable protic ionic liquids as solvent-catalysts for improved synthesis of multiply substituted 1,2,4-triazoles from oxadiazoles and organoamines

More than green alternatives to traditional volatile molecular organic solvents, protic ionic liquids as dual solvent-catalysts have been successfully used to promote reactions of organoamines with oxadiazoles to afford sterically hindered 1,2,4-triazoles. Among the tested protic ionic liquids, pyridinium trifluoroacetate and acetate showed the highest efficiency for the reactions of arylamines and alkylamines, respectively, indicating that tunable catalysis could be readily effected with protic ionic liquid solvent-catalysts by simply tuning their cation and anion counterparts. A general and efficient approach has been developed for synthesis of multiply substituted 1,2,4-triazoles based on the tunable protic ionic liquid solvent-catalyst systems.

Microwave-assisted and efficient one-pot synthesis of substituted 1,2,4-triazoles

An efficient microwave-assisted one-pot and three-component synthesis of substituted 1,2,4-triazoles has been achieved utilizing substituted primary amines.