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2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole

Base Information Edit
  • Chemical Name:2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole
  • CAS No.:279250-86-1
  • Molecular Formula:C7H4F3N3S
  • Molecular Weight:219.19
  • Hs Code.:
  • Mol file:279250-86-1.mol
2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole

Synonyms:

Suppliers and Price of 2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole
Supply Marketing:Edit
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
  • Matrix Scientific
  • 2-(4-Trifluoromethyl-1H-imidazol-2-yl)-thiazole 95%
  • 2.500g
  • $ 1403.00
  • AccelPharmtech
  • 2-[5-(trifluoromethyl)-1H-imidazol-2-yl]-Thiazole 97.00%
  • 1G
  • $ 1940.00
Total 0 raw suppliers
Chemical Property of 2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole Edit
Chemical Property:
Purity/Quality:

2-(4-Trifluoromethyl-1H-imidazol-2-yl)-thiazole 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole

There total 1 articles about 2-(2-thiazolyl)-4-trifluoromethyl-1H-imidazole 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:
Guidance literature:
1,1-dibromo-3,3,3-trifluoroacetone; With sodium acetate; for 0.5h; Heating;
Thiazole-2-carbaldehyde; With ammonium hydroxide; In methanol; at 20 ℃; for 20h;
DOI:10.1021/jm991154w
Guidance literature:
With ammonium hydroxide; In methanol; at 60 ℃; for 24h;
DOI:10.1021/jm991154w
Guidance literature:
Multi-step reaction with 2 steps
1: 76 percent / aq. NH3 / methanol / 24 h / 60 °C
2: 45 percent / DIBALH / tetrahydrofuran; toluene / -78 - 0 °C
With ammonium hydroxide; diisobutylaluminium hydride; In tetrahydrofuran; methanol; toluene; 1: Substitution / 2: Reduction;
DOI:10.1021/jm991154w
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