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Tizoxanide

Base Information Edit
  • Chemical Name:Tizoxanide
  • CAS No.:173903-47-4
  • Molecular Formula:C10H7N3O4S
  • Molecular Weight:265.249
  • Hs Code.:
  • European Community (EC) Number:827-733-6
  • NSC Number:697856
  • UNII:15KFG88UOJ
  • DSSTox Substance ID:DTXSID40169680
  • Nikkaji Number:J772.210I
  • Wikipedia:Tizoxanide
  • Wikidata:Q6587134
  • ChEMBL ID:CHEMBL1545
  • Mol file:173903-47-4.mol
Tizoxanide

Synonyms:tizoxanide

Suppliers and Price of Tizoxanide
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
  • Usbiological
  • Tizoxanide
  • 25mg
  • $ 460.00
  • TRC
  • Tizoxanide
  • 25mg
  • $ 160.00
  • TCI Chemical
  • Tizoxanide
  • 25MG
  • $ 124.00
  • TCI Chemical
  • Tizoxanide
  • 100MG
  • $ 339.00
  • Medical Isotopes, Inc.
  • Tizoxanide 98%
  • 10 mg
  • $ 900.00
  • Matrix Scientific
  • 2-Hydroxy-N-(5-nitrothiazol-2-yl)benzamide 95+%
  • 5g
  • $ 924.00
  • Matrix Scientific
  • 2-Hydroxy-N-(5-nitrothiazol-2-yl)benzamide 95+%
  • 1g
  • $ 341.00
  • J&W Pharmlab
  • Tizoxanide 97%
  • 250mg
  • $ 129.00
  • J&W Pharmlab
  • Tizoxanide 97%
  • 1g
  • $ 158.00
  • J&W Pharmlab
  • Tizoxanide 97%
  • 100mg
  • $ 98.00
Total 30 raw suppliers
Chemical Property of Tizoxanide Edit
Chemical Property:
  • Melting Point:279-281°(dec) 
  • PKA:6.70±0.50(Predicted) 
  • PSA:136.28000 
  • Density:1.644±0.06 g/cm3(Predicted) 
  • LogP:2.60540 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:DMSO (Slightly), Methanol (Slightly, Heated) 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:2
  • Exact Mass:265.01572689
  • Heavy Atom Count:18
  • Complexity:336
Purity/Quality:

99% *data from raw suppliers

Tizoxanide *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C(=C1)C(=O)NC2=NC=C(S2)[N+](=O)[O-])O
  • Description Tizoxanide is an active metabolite of the antiparasitic nitazoxanide . Tizoxanide is formed from nitazoxanide via deacetylation of nitazoxanide in the stomach. It is active against M. tuberculosis (MIC = 16 μg/ml). It also reduces the growth of the disease-causing parasites L. mexicana and T. cruzi in vitro (IC50s = 6.2 and 17.5 μM, respectively), inhibits influenza A replication (EC50s = 0.3-1 μM), and inhibits hepatitis B and hepatitis C virus replication (EC50 = 0.15 μM for both).
  • Uses A metabolite of Nitazoxanide; a potent inhibitor of hepatitis B virus and hepatitis C virus. A metabolite of Nitazoxanide (N490100); a potent inhibitor of hepatitis B virus and hepatitis C virus. A metabolite of Nitazoxanide (N490100); a potent inhibitor of hepatitis B virus and hepatitis C virus. Kills Mycobacterium tuberculosis.
Technology Process of Tizoxanide

There total 3 articles about Tizoxanide 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 hydrogenchloride; at 50 ℃; for 24h;
DOI:10.1039/a806676k
Guidance literature:
With lithium chloride; In N,N-dimethyl-formamide; at 130 ℃; for 3h;
Guidance literature:
Multi-step reaction with 2 steps
1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C
2: lithium chloride / N,N-dimethyl-formamide / 3 h / 130 °C
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; lithium chloride; In N,N-dimethyl-formamide;
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