60406-74-8

Basic information

• Product Name: 4H-1,2,4-Triazole, 4-[4-(1,1-dimethylethyl)phenyl]-3-(trifluoromethyl)-
• CAS NO: 60406-74-8
• Molecular Formula: C13H14F3N3
• Molecular Weight: 269.269
• Mol File: 60406-74-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4H-1,2,4-Triazole, 4-[4-(1,1-dimethylethyl)phenyl]-3-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,2,4-Triazole, 4-[4-(1,1-dimethylethyl)phenyl]-3-(trifluoromethyl)-(60406-74-8)
• EPA Substance Registry System: 4H-1,2,4-Triazole, 4-[4-(1,1-dimethylethyl)phenyl]-3-(trifluoromethyl)-(60406-74-8)

Safety Data

• Hazardous Substances Data: 60406-74-8(Hazardous Substances Data)

Upstream product

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Relevant articles and documents

Method for synthesizing 3-trifluoromethyl substituted 1,2,4-triazole compounds by taking glucose as carbon source

The invention discloses a preparation method of 3-trifluoromethyl substituted 1,2,4-triazole compounds, wherein the preparation method comprises the following steps: adding trifluoromethanesulfonic acid, a 70% aqueous solution of tert-butyl hydroperoxide, water, trifluoroethyl imine hydrazide and glucose into an organic solvent, reacting at the temperature of 70-90 DEG C for 2-4 hours, and after the reaction is completed, carrying out post-treatment to obtain the 3-trifluoromethyl substituted 1,2,4-triazole compounds. The preparation method has the advantages of mild conditions, simple operation, no need of anhydrous and anaerobic conditions, simple and easily available initial raw materials, especially glucose is a biomass raw material widely existing in the nature, the reaction efficiency is high, the reaction can be expanded to gram-level reaction, 1,2,4-triazole compounds having trifluoromethyl groups and substituted by different functional groups can also be synthesized through substrate design, and the applicability of the method is widened while the operation is convenient.

Preparation method of 3-trifluoromethyl substituted 1,2,4-triazole compound

The invention discloses a preparation method of a 3-trifluoromethyl substituted 1,2,4-triazole compound. The preparation method comprises the following steps: adding molybdenum hexacarbonyl, cuprous acetate, triethylamine, a molecular sieve, trifluoroethy

Acaricidal trifluoromethyl-1,2,4-triazoles

3-Trihalomethyl-1,2,4-triazoles either unsubstituted or having substituents in the 4 and/or 5, 1 and/or 5, and 2 and/or 5 positions; and methods for their preparation. Some of the compounds show biological activity; others have acaricidal activity.