41217-48-5

Basic information

• Product Name: 1H-1,2,4-Triazole, 3,5-dimethyl-1-phenyl-
• CAS NO: 41217-48-5
• Molecular Formula: C10H11N3
• Molecular Weight: 173.217
• Mol File: 41217-48-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1H-1,2,4-Triazole, 3,5-dimethyl-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-1,2,4-Triazole, 3,5-dimethyl-1-phenyl-(41217-48-5)
• EPA Substance Registry System: 1H-1,2,4-Triazole, 3,5-dimethyl-1-phenyl-(41217-48-5)

Safety Data

• Hazardous Substances Data: 41217-48-5(Hazardous Substances Data)

Upstream product

• 625-77-4 N-acetylacetamide 
• 59-88-1 phenylhydrazine hydrochloride 
• 55-21-0 benzamide 
• 114-83-0 1-acetyl-2-phenylhydrazine 
• 75-07-0 acetaldehyde 
• 81549-01-1 1-Phenylazo-ethylamine 
• 118559-38-9 N-(1-Nitroethylidene)-N'-phenyl-N'-sodiohydrazine 
• 23326-27-4 Methyl 2-butynoate 
• 100-63-0 phenylhydrazine 
• 75-05-8 acetonitrile 
• 100-42-5 styrene 
• 60-35-5 acetamide 
• 532-96-7 N-benzoyl-N'-phenylhydrazine 

Downstream Products

• 109567-01-3 3-ethyl-5-[(4,5-dimethyl-2-phenyl-2,4-dihydro-[1,2,4]triazol-3-yliden)-ethylidene]-2-thioxo-thiazolidin-4-one 
• 123055-70-9 1-(1-ethyl-[2]quinolyl)-3-(4,5-dimethyl-2-phenyl-2H-[1,2,4]triazol-3-yl)-trimethinium ; iodide 
• 41316-57-8 3,4,5-trimethyl-1-phenyl-[1,2,4]triazolium; iodide 
• 112351-77-6 4-[(4,5-dimethyl-2-phenyl-2,4-dihydro-[1,2,4]triazol-3-yliden)-ethylidene]-2-phenyl-4H-oxazol-5-one 

Relevant articles and documents

Synthesis of 1,3,5-trisubstituted-1,2,4-triazoles by microwave-assisted N-acylation of amide derivatives and the consecutive reaction with hydrazine hydrochlorides

Facile and efficient procedures for the N-acylation reaction of amide derivatives with various acid anhydrides and the cyclization reaction of N-acylated amide derivatives with various hydrazine hydrochlorides were described. The reactions were carried out under microwave irradiation to give products in good yields in a few minutes. The synthesis of 1,3,5-trisubstituted- 1,2,4-triazoles from benzamides can also be accomplished in a simple one-pot sequential reaction.

Simple route for the synthesis of 1,3,5-tri-substituted-s-triazoles

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Synthese et reactivite de quelques α-amino azocomposes: mecanisme de la cyclisation thermique en triazoles-1,2,4

The reaction of O-mesitylenesulfonylhydroxylamine (MSH) with hydrazones leads to carbon amination with the formation of α-amino azo compounds.Thermolysis of these compounds affords 1,2,4-triazoles.The mechanism of this cyclization is discussed.