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2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine

Base Information
  • Chemical Name:2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine
  • CAS No.:121358-21-2
  • Molecular Formula:C11H13N5O5
  • Molecular Weight:295.255
  • Hs Code.:
  • Mol file:121358-21-2.mol
2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine

Synonyms:2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine

Suppliers and Price of 2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine
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 2 raw suppliers
Chemical Property of 2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine
Chemical Property:
  • PSA:156.61000 
  • LogP:-1.76300 
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
Technology Process of 2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine

There total 5 articles about 2-Carbamyl-9-[beta-d-ribofuranosyl]hypoxanthine 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 sodium hydroxide; dihydrogen peroxide; In ethanol; for 1h;
DOI:10.1016/S0040-4020(01)86068-3
Guidance literature:
Multi-step reaction with 5 steps
1: 37 percent / n-pentyl nitrite / acetonitrile / 12 h / Heating
2: 1) NaOMe 2) NH4Cl / 1) methanol, 1h; 2) methanol, 1 h
3: 74 percent / KHSO5 / 12 h / 0 °C / acetate buffer, pH = 4.2
4: 40 percent / dimethylformamide / 15 h / 0 °C
5: 34 percent / NaOH, H2O2 (30percent) / ethanol / 1 h
With sodium hydroxide; potassium peroxomonosulfate; n-Amyl nitrite; dihydrogen peroxide; sodium methylate; ammonium chloride; In ethanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/S0040-4020(01)86068-3
Guidance literature:
Multi-step reaction with 4 steps
1: 1) NaOMe 2) NH4Cl / 1) methanol, 1h; 2) methanol, 1 h
2: 74 percent / KHSO5 / 12 h / 0 °C / acetate buffer, pH = 4.2
3: 40 percent / dimethylformamide / 15 h / 0 °C
4: 34 percent / NaOH, H2O2 (30percent) / ethanol / 1 h
With sodium hydroxide; potassium peroxomonosulfate; dihydrogen peroxide; sodium methylate; ammonium chloride; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)86068-3
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