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Norsecurinine

Base Information
  • Chemical Name:Norsecurinine
  • CAS No.:2650-35-3
  • Molecular Formula:C12H13 N O2
  • Molecular Weight:203.23712
  • Hs Code.:
  • UNII:OPF6A516XH
  • DSSTox Substance ID:DTXSID40949368
  • Nikkaji Number:J15.086J
  • Wikipedia:Norsecurinine
  • Wikidata:Q104399056
  • Mol file:2650-35-3.mol
Norsecurinine

Synonyms:ent-norsecurinine;nor-securinine;norsecurinine

Suppliers and Price of Norsecurinine
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
  • TRC
  • NorSecurinine
  • 25mg
  • $ 24750.00
Total 9 raw suppliers
Chemical Property of Norsecurinine
Chemical Property:
  • Vapor Pressure:2E-08mmHg at 25°C 
  • Boiling Point:453.8°C at 760 mmHg 
  • Flash Point:200.9°C 
  • PSA:29.54000 
  • Density:1.35g/cm3 
  • LogP:0.95280 
  • XLogP3:0.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:0
  • Exact Mass:203.094628657
  • Heavy Atom Count:15
  • Complexity:412
Purity/Quality:

99% *data from raw suppliers

NorSecurinine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2C34CC(N2C1)C=CC3=CC(=O)O4
  • Isomeric SMILES:C1C[C@@H]2[C@]34C[C@H](N2C1)C=CC3=CC(=O)O4
  • Uses A new alkaloid from Phyllanthus niruri. A new alkaloid from Phyllanthus niruri. These alkaloids have found a sporadic use clinically for such diseases as poliomyelitis, ALS (amyotrophic lateral sclerosis) and chronic aplastic anemia.
Technology Process of Norsecurinine

There total 78 articles about Norsecurinine 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 di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20 ℃; for 3h; Inert atmosphere;
DOI:10.1002/chem.201903122
Guidance literature:
With dmap; methanesulfonyl chloride; triethylamine; In dichloromethane; for 0.25h;
DOI:10.1016/S0040-4020(01)88027-3
Guidance literature:
With silver hexafluoroantimonate; In acetone; at 20 ℃; Inert atmosphere;
DOI:10.1002/anie.201208261
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