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cytarazid

Base Information
  • Chemical Name:cytarazid
  • CAS No.:67013-98-3
  • Molecular Formula:C9H12N6O4
  • Molecular Weight:268.2294
  • Hs Code.:
  • Mol file:67013-98-3.mol
cytarazid

Synonyms:cytarazid;1-(2-azido-2-deoxy-β-D-arabinofuranosyl) cytosine;1-(2-azido-2-deoxy-β-D-arabinofuranosyl)-cytosine;

Suppliers and Price of cytarazid
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
  • American Custom Chemicals Corporation
  • CYTARAZID 95.00%
  • 5MG
  • $ 502.24
Total 2 raw suppliers
Chemical Property of cytarazid
Chemical Property:
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • PSA:160.35000 
  • Density:g/cm3 
  • LogP:-1.21104 
Purity/Quality:

98% *data from raw suppliers

CYTARAZID 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of cytarazid

There total 11 articles about cytarazid 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 tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.75h;
DOI:10.1021/jm00107a018
Guidance literature:
Multi-step reaction with 3 steps
1: phosphoryl oxychloride, triethylamine / acetonitrile
2: NH4OH
3: 80 percent / tetrabutylammonium fluoride
With ammonium hydroxide; tetrabutyl ammonium fluoride; phosphoryl oxychloride on N,N-dimethylformamide; triethylamine; In acetonitrile;
DOI:10.1248/cpb.37.1659
Guidance literature:
Multi-step reaction with 5 steps
1: 70 percent / diethyl azodicarboxylate, triphenyl phosphorazidate, triphenylphosphine / tetrahydrofuran / 4 h / Ambient temperature
2: 94 percent / concd. NH4OH / methanol / 1.5 h / Ambient temperature
3: tetrabutylammonium bromide, 0.2 M aq. NaHCO3 / CH2Cl2 / 6.5 h / Ambient temperature
4: concd. NH4OH / dioxane / Ambient temperature
5: 100 percent / tetrabutylammonium fluoride (TBAF) / tetrahydrofuran / 0.75 h / 0 °C
With ammonium hydroxide; diphenylphosphoranyl azide; tetrabutyl ammonium fluoride; tetrabutylammomium bromide; sodium hydrogencarbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane;
DOI:10.1021/jm00107a018
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