4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Base Information

Chemical Name:4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole
CAS No.:1607441-83-7
Molecular Formula:C₁₇H₁₁F₆N₃O₂
Molecular Weight:403.284
Hs Code.:

Synonyms:4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Suppliers and Price of 4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

There total 7 articles about 4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 1607442-71-6
4-(bromomethyl)-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

: 1607441-83-7
4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In ethanol; at 23 ℃; for 6h; Inert atmosphere;

Reference yield:

: 1607442-67-0
ethyl 5-[3-(trifluoromethoxy)phenoxy]-2H-1,2,3-triazole-4-carboxylate

: 1607441-83-7
4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 80 °C

2.1: sodium dithionite / water; acetonitrile / 2 h / 23 °C

3.1: sulfuric acid; isopentyl nitrite / ethanol / 1 h / -20 °C

3.2: 14 h / 23 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.33 h / 0 °C

5.1: acetic acid; hydrogen bromide / water / 4 h / Reflux

6.1: hydrogen; 5%-palladium/activated carbon / ethanol / 6 h / 23 °C / Inert atmosphere

With lithium aluminium tetrahydride; sodium dithionite; sulfuric acid; 5%-palladium/activated carbon; hydrogen bromide; hydrogen; potassium carbonate; acetic acid; isopentyl nitrite; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 367-86-2
1-fluoro-2-nitro-4-trifluoromethyl-benzene

: 1607441-83-7
4-methyl-5-[3-(trifluoromethoxy)phenoxy]-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 1.5 h / 80 °C

2.1: sodium dithionite / water; acetonitrile / 2 h / 23 °C

3.1: sulfuric acid; isopentyl nitrite / ethanol / 1 h / -20 °C

3.2: 14 h / 23 °C

4.1: lithium aluminium tetrahydride / tetrahydrofuran / 0.33 h / 0 °C

5.1: acetic acid; hydrogen bromide / water / 4 h / Reflux

6.1: hydrogen; 5%-palladium/activated carbon / ethanol / 6 h / 23 °C / Inert atmosphere

With lithium aluminium tetrahydride; sodium dithionite; sulfuric acid; 5%-palladium/activated carbon; hydrogen bromide; hydrogen; potassium carbonate; acetic acid; isopentyl nitrite; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile;