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6N-HydroxyMethyl Tenofovir Disoproxil

Base Information
  • Chemical Name:6N-HydroxyMethyl Tenofovir Disoproxil
  • CAS No.:1244022-53-4
  • Molecular Formula:C20H32N5O11P
  • Molecular Weight:549.468741
  • Hs Code.:
  • Mol file:1244022-53-4.mol
6N-HydroxyMethyl Tenofovir Disoproxil

Synonyms:6N-HydroxyMethyl Tenofovir Disoproxil;6N-HydroxyMethyl Tenofovir Disoproxil Discontinued See: M264450;(R)-(((((1-(6-((hydroxymethyl)amino)-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphoryl)bis(oxy))bis(methylene) diisopropyl bis(carbonate)

Suppliers and Price of 6N-HydroxyMethyl Tenofovir Disoproxil
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 10 raw suppliers
Chemical Property of 6N-HydroxyMethyl Tenofovir Disoproxil
Chemical Property:
  • Boiling Point:687.9±65.0 °C(Predicted) 
  • PKA:13.41±0.10(Predicted) 
  • PSA:201.49000 
  • Density:1.45±0.1 g/cm3(Predicted) 
  • LogP:2.88810 
  • Storage Temp.:Refrigerator 
  • Solubility.:Dichloromethane, Ethyl Acetate 
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses Intermediate in the preparation of Tenofovir Disoproxil Fumarate (T018505).
Technology Process of 6N-HydroxyMethyl Tenofovir Disoproxil

There total 5 articles about 6N-HydroxyMethyl Tenofovir Disoproxil 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 formic acid; In acetonitrile; at 50 - 70 ℃; Inert atmosphere;
Guidance literature:
tenofovir; With triethylamine; In 1-methyl-pyrrolidin-2-one; at 45 ℃;
chloromethyl isopropyl carbonate; With tetrabutylammomium bromide; In 1-methyl-pyrrolidin-2-one; at 45 - 50 ℃; for 5.5h;
DOI:10.1021/op1001337
Guidance literature:
Multi-step reaction with 4 steps
1.1: sodium hydroxide / N,N-dimethyl-formamide / 120 °C
2.1: magnesium 2-methylpropan-2-olate / 1-methyl-pyrrolidin-2-one / 70 - 74 °C
3.1: chloro-trimethyl-silane; sodium bromide / 1-methyl-pyrrolidin-2-one / 0 - 75 °C
4.1: triethylamine / 1-methyl-pyrrolidin-2-one / 45 °C
4.2: 5.5 h / 45 - 50 °C
With chloro-trimethyl-silane; magnesium 2-methylpropan-2-olate; triethylamine; sodium bromide; sodium hydroxide; In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide;
DOI:10.1021/op1001337
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