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Ribavirin 5'-sulfamate

Base Information
  • Chemical Name:Ribavirin 5'-sulfamate
  • CAS No.:120615-22-7
  • Molecular Formula:C8H13N5O7S
  • Molecular Weight:323.287
  • Hs Code.:
  • DSSTox Substance ID:DTXSID60152933
  • Nikkaji Number:J271.464G
  • Wikidata:Q83019728
  • Mol file:120615-22-7.mol
Ribavirin 5'-sulfamate

Synonyms:1-(5'-O-sulfamoyl-beta-ribofuranosyl)-(1,2,4)triazole-3-carboxamide;5'-O-sulfamoyl-1-ribofuranosyl-1,2,4-triazole-3-carboxamide;ribavirin 5'-sulfamate

Suppliers and Price of Ribavirin 5'-sulfamate
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
  • RIBAVIRIN 5'-SULFAMATE 95.00%
  • 5MG
  • $ 499.83
Total 1 raw suppliers
Chemical Property of Ribavirin 5'-sulfamate
Chemical Property:
  • Boiling Point:729.2°Cat760mmHg 
  • Flash Point:394.8°C 
  • PSA:201.26000 
  • Density:2.25g/cm3 
  • LogP:-1.30230 
  • XLogP3:-3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:10
  • Rotatable Bond Count:5
  • Exact Mass:323.05356894
  • Heavy Atom Count:21
  • Complexity:496
Purity/Quality:

RIBAVIRIN 5'-SULFAMATE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=NC(=NN1C2C(C(C(O2)COS(=O)(=O)N)O)O)C(=O)N
  • Isomeric SMILES:C1=NC(=NN1[C@H]2[C@@H]([C@@H]([C@H](O2)COS(=O)(=O)N)O)O)C(=O)N
Technology Process of Ribavirin 5'-sulfamate

There total 4 articles about Ribavirin 5'-sulfamate 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:
Multi-step reaction with 3 steps
1: 58 percent / 70percent perchloric acid / acetone / 1.5 h / 0 °C
2: 1.) NaH / 1.) THF, 0 deg C, 15 min, 2.) a.) 0 deg C, 2 h, b.) RT, 4 h
3: 93 percent / 80percent acetic acid / 2 h / 100 °C
With perchloric acid; sodium hydride; acetic acid; In acetone;
DOI:10.1021/jm00163a008
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