13576-46-0

Basic information

• Product Name: 3,5-dimethyl-4-phenyl-4H-[1,2,4]triazole
• Synonyms: 3,5-dimethyl-4-phenyl-4H-[1,2,4]triazole
• CAS NO: 13576-46-0
• Molecular Weight: 173.217
• Mol File: 13576-46-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3,5-dimethyl-4-phenyl-4H-[1,2,4]triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-dimethyl-4-phenyl-4H-[1,2,4]triazole(13576-46-0)
• EPA Substance Registry System: 3,5-dimethyl-4-phenyl-4H-[1,2,4]triazole(13576-46-0)

Safety Data

• Hazardous Substances Data: 13576-46-0(Hazardous Substances Data)

Upstream product

• 13148-65-7 2,5-dimethyl-1,3,4-oxadiazole 
• 62-53-3 aniline 
• 18871-66-4 N,N-dimethylacetamide dimethyl acetal 
• 1068-57-1 acetic acid hydrazide 
• 1286211-01-5 C₈H₁₁N₃ 
• 108-24-7 acetic anhydride 
• 103-84-4 Acetanilid 
• 637-53-6 thioacetanilide 
• 58010-97-2 N-acetyl-N'-formyl-hydrazine 

Downstream Products

• 41217-51-0 1,3,5-trimethyl-4-phenyl-[1,2,4]triazolium; iodide 
• 39753-99-6 3-ethyl-5-methyl-4-phenyl-1,2,4-triazole 
• 142506-27-2 3-(2-hydroxy-2-methyl-1-propyl)-5-methyl-4-phenyl-1,2,4-triazole 
• 142506-28-3 (R,S)-3-((1-hydroxy-1,2,3,4-tetrahydro-1-naphthyl)methyl)-5-methyl-4-phenyl-1,2,4-triazole 

Relevant articles and documents

HClO4-SiO2: An efficient reusable catalyst for the synthesis of 3,4,5-trisubstituted 1,2,4-triazoles under solvent-free conditions

A series of 3,4,5-trisubstituted 1,2,4-triazoles have been synthesized from N3-substituted amidrazones and anhydrides using HClO 4-SiO2 at 80 °C under solvent-free conditions. The products were obtained in excellent yields

Efficient and regiospecific one-pot synthesis of substituted 1,2,4-triazoles

(Equation Presented) An efficient one-pot, three-component synthesis of substituted 1,2,4-triazoles has been developed, utilizing a wide range of substituted primary amines and acyl hydrazides.