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

Encyclopedia

2-bromo-6-(4-nitrophenylethoxy)purine

Base Information Edit
  • Chemical Name:2-bromo-6-(4-nitrophenylethoxy)purine
  • CAS No.:127244-78-4
  • Molecular Formula:C13H10BrN5O3
  • Molecular Weight:364.158
  • Hs Code.:
  • Mol file:127244-78-4.mol
2-bromo-6-(4-nitrophenylethoxy)purine

Synonyms:2-bromo-6-(4-nitrophenylethoxy)purine

Suppliers and Price of 2-bromo-6-(4-nitrophenylethoxy)purine
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 2-bromo-6-(4-nitrophenylethoxy)purine Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-bromo-6-(4-nitrophenylethoxy)purine

There total 1 articles about 2-bromo-6-(4-nitrophenylethoxy)purine 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 acetic acid; triethylamine; triphenylphosphine; diethylazodicarboxylate; Yield given. Title compound not separated from byproducts; 1.) 100 deg C, 2 h; 2.) dioxane, 80 deg C, 6 h; 3.) 80 deg C;
DOI:10.1039/c39890001769
Guidance literature:
Multi-step reaction with 4 steps
2: 95 percent / CF3SO3SiMe3 / acetonitrile / reflux, 1h; rt, 16 h
3: 1,8-diazabicyclo<5.4.0>undec-7-ene / acetonitrile
4: 80 percent / NH3 / methanol / 120 °C
With trimethylsilyl trifluoromethanesulfonate; ammonia; 1,8-diazabicyclo[5.4.0]undec-7-ene; In methanol; acetonitrile;
DOI:10.1039/c39890001769
Guidance literature:
Multi-step reaction with 4 steps
2: 95 percent / CF3SO3SiMe3 / acetonitrile / reflux, 1h; rt, 16 h
3: 1,8-diazabicyclo<5.4.0>undec-7-ene / acetonitrile
4: hydrogen / Pd/C / 16 h / 3102.9 Torr / Ambient temperature
With trimethylsilyl trifluoromethanesulfonate; hydrogen; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium on activated charcoal; In acetonitrile;
DOI:10.1039/c39890001769
Refernces Edit
Post RFQ for Price