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Fluoroazomycin arabinoside

Base Information
  • Chemical Name:Fluoroazomycin arabinoside
  • CAS No.:220793-03-3
  • Molecular Formula:C8H10FN3O5
  • Molecular Weight:247.183
  • Hs Code.:
  • UNII:1QR3UU6P48
  • Nikkaji Number:J1.050.259D
  • Wikidata:Q27252764
  • ChEMBL ID:CHEMBL589255
  • Mol file:220793-03-3.mol
Fluoroazomycin arabinoside

Synonyms:(18F)-1-alpha-D-(2-deoxy-2-fluoroarabinofuranosyl)-2-nitroimidazole;(18F)-FAZA;(18F)FAZA;(18F)fluoro-azomycinarabino-furanoside;(18F)fluoroazomycinarabinoside;18F-FAZA;18F-fluoroazomycin arabinoside;fluoroazomycin arabinoside;fluoroazomycinarabinoside

Suppliers and Price of Fluoroazomycin arabinoside
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
  • Biosynth Carbosynth
  • 1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole
  • 50 mg
  • $ 3500.00
  • Biosynth Carbosynth
  • 1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole
  • 20 mg
  • $ 1700.00
  • Biosynth Carbosynth
  • 1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole
  • 10 mg
  • $ 950.00
  • Biosynth Carbosynth
  • 1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole
  • 5 mg
  • $ 625.00
  • Biosynth Carbosynth
  • 1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole
  • 2 mg
  • $ 350.00
Total 8 raw suppliers
Chemical Property of Fluoroazomycin arabinoside
Chemical Property:
  • PSA:113.33000 
  • LogP:-0.09680 
  • XLogP3:-0.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:2
  • Exact Mass:247.06044859
  • Heavy Atom Count:17
  • Complexity:301
Purity/Quality:

99.3% *data from raw suppliers

1-(5'-Deoxy-5'-fluoro-a-D-arabinofuranosyl)-2-nitroimidazole *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CN(C(=N1)[N+](=O)[O-])C2C(C(C(O2)CF)O)O
  • Isomeric SMILES:C1=CN(C(=N1)[N+](=O)[O-])[C@@H]2[C@H]([C@@H]([C@H](O2)CF)O)O
  • Recent ClinicalTrials:The Potential for Metformin to Improve Tumor Oxygenation in Locally Advanced Cervix Cancer: A Phase II Randomized Trial
  • Recent EU Clinical Trials:THE ROLE OF 18F-FAZA PET IMAGING TECHNIQUE IN DETECTING LYMPH NODE METASTASES IN RENAL CELL CARCINOMA PATIENTS
Technology Process of Fluoroazomycin arabinoside

There total 20 articles about Fluoroazomycin arabinoside 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 ammonia; In methanol; at 0 - 4 ℃; Inert atmosphere;
DOI:10.1016/j.jfluchem.2013.06.013
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