Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

6,7-dimethyl-2-phenylbenzo[d]thiazole

Base Information Edit
  • Chemical Name:6,7-dimethyl-2-phenylbenzo[d]thiazole
  • CAS No.:1620817-52-8
  • Molecular Formula:C15H13NS
  • Molecular Weight:239.341
  • Hs Code.:
  • Mol file:1620817-52-8.mol
6,7-dimethyl-2-phenylbenzo[d]thiazole

Synonyms:6,7-dimethyl-2-phenylbenzo[d]thiazole

Suppliers and Price of 6,7-dimethyl-2-phenylbenzo[d]thiazole
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
Total 0 raw suppliers
Chemical Property of 6,7-dimethyl-2-phenylbenzo[d]thiazole Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 6,7-dimethyl-2-phenylbenzo[d]thiazole

There total 3 articles about 6,7-dimethyl-2-phenylbenzo[d]thiazole 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:
With sulfur; di-μ-hydroxo-bis[(N,N,N′,N′-tetramethylethylenediamine)copper(II)] chloride; oxygen; In dimethyl sulfoxide; at 100 ℃; for 24h; under 760.051 Torr; Overall yield = 62 percent; Overall yield = 73.6 mg;
DOI:10.1002/adsc.202000598
Guidance literature:
With p-nitrobenzene iodide; Oxone; trifluorormethanesulfonic acid; at 20 ℃; for 12h; Overall yield = 75 %; Overall yield = 65 mg; Green chemistry;
DOI:10.1021/jo501216h
Guidance literature:
Multi-step reaction with 2 steps
1: Lawessons reagent
2: p-nitrobenzene iodide; trifluorormethanesulfonic acid; Oxone / 12 h / 20 °C / Green chemistry
With Lawessons reagent; p-nitrobenzene iodide; Oxone; trifluorormethanesulfonic acid;
DOI:10.1021/jo501216h
Post RFQ for Price