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Namitecan

Base Information
  • Chemical Name:Namitecan
  • CAS No.:372105-27-6
  • Molecular Formula:C23H22N4O5
  • Molecular Weight:434.451
  • Hs Code.:
  • UNII:X34Z8N66T3
  • DSSTox Substance ID:DTXSID90190707
  • Nikkaji Number:J2.022.769I
  • NCI Thesaurus Code:C95910
  • Metabolomics Workbench ID:153170
  • ChEMBL ID:CHEMBL419186
Namitecan

Synonyms:namitecan;ST 1968;ST-1968;ST1968

Suppliers and Price of Namitecan
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
  • ChemScene
  • Namitecan 98.11%
  • 5mg
  • $ 500.00
  • ChemScene
  • Namitecan 98.11%
  • 1mg
  • $ 245.00
  • ChemScene
  • Namitecan 98.11%
  • 50mg
  • $ 2550.00
  • ChemScene
  • Namitecan 98.11%
  • 10mg
  • $ 850.00
  • American Custom Chemicals Corporation
  • NAMITECAN 95.00%
  • 5MG
  • $ 500.06
Total 3 raw suppliers
Chemical Property of Namitecan
Chemical Property:
  • Boiling Point:835.2±75.0 °C(Predicted) 
  • Density:1.51±0.1 g/cm3(Predicted) 
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:5
  • Exact Mass:434.15901982
  • Heavy Atom Count:32
  • Complexity:899
Purity/Quality:

≥98% *data from raw suppliers

Namitecan 98.11% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:CCC1(C2=C(COC1=O)C(=O)N3CC4=C(C5=CC=CC=C5N=C4C3=C2)C=NOCCN)O
  • Isomeric SMILES:CC[C@@]1(C2=C(COC1=O)C(=O)N3CC4=C(C5=CC=CC=C5N=C4C3=C2)/C=N/OCCN)O
  • Recent ClinicalTrials:ST1968 Intravenous (Weekly) in Solid Tumors
Technology Process of Namitecan

There total 3 articles about Namitecan 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 pyridine; In ethanol; for 3h; Title compound not separated from byproducts.; Heating;
DOI:10.1021/jm0108092
Guidance literature:
With pyridine; In ethanol; for 3h; Title compound not separated from byproducts.; Heating;
DOI:10.1021/jm0108092
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